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Showing posts with label Economic justification. Show all posts
Showing posts with label Economic justification. Show all posts

Wednesday, November 7, 2018

Quick Review of Chemicals Related Process Development, Design and Scale up Considerations

Chemical engineers and chemists are the Picasso, the Michelangelo, the Zaha Hadid or the Gaudí or other artisans of their process designs. Their designs are emblematic of their learning, creativity and imagination. They use their training including their capabilities to exploit mutual behavior of chemicals and creatively extend  equipment performance to design excellent economic processes. 

Process development from the laboratory to a commercial operation goes through many similar steps. There is a process we all are aware of and go through, some cited (1,2,3). However, it is always good to re-visit the process and brush up on what we have learnt and are practicing (4). Such reviews lead to creativity sparks and eureka moments to do better. Learning never ends and has been covered by many to cite.

Below is a quick review from the lab to commercial path and steps we took and have since continuously improved. Steps are simple but as said earlier need to be revisited and improved. There is not enough space to cover everything. Please don’t be offended if I have overlooked few things. There is no financial involvement or remuneration from the companies cited. They are just examples.   

Most of us go through all or some variations of the following generic steps. 

1.    Commercial value of a chemical or formulation product is identified.
2.    A cost analysis is done and compared to any similar product on the market. If the cost and performance are better than the existing product/s, commercial value is explored/developed. If there are no similar products companies work fast to establish their foothold. 
3.    Product’s synthetic/formulation route is developed on paper, costed and explored in a laboratory.
4.    Time is spent to come up with the best operating conditions and the highest yield. Process is optimized. Additional cost analysis is done while the process development work is underway.  

With each positive in the above, race accelerates to commercialize the product. In process development subtle simplification steps can be overlooked. They can have significant impact on the product’s success. List is long but I am sharing some of the key steps that I have practiced. I am sure there are other ideas that are used. 

Raw Materials: 

Well accepted common practice in the lab is to get the raw materials from known research supply companies. For the initial steps, this might be alright but for the long-term success, it is of utmost importance to source the raw materials from commercial producers. Raw materials from the research supply companies are expensive and too pure to give any credible data and value for a commercial product. By getting the raw materials from commercial producers not only the developer company establishes a relationship and a long-term value but is also dealing with real raw materials that give us a dose of reality to develop an optimum and economic process. 

Acquisition of raw materials is different for batch and continuous process. Raw materials of batch process can be acquired when needed but for every continuous process they have to be available all the time. In either case raw materials don’t have to be tested prior to use if the laid-out needs are clearly defined and there is trust in supplier’s quality. Any deviation in raw materials from the established standard can spell significant financial loss especially for the continuous process.   

Physical State:

We all know that each raw material has its established physical properties and has its own specific behavior towards other chemicals including reaction by-products and products. How we understand these nuances and capitalize on their mutual behavior is critical for process development. Even with this acknowledged, still there are challenges we have to deal with. 

Physical state of each raw material and each reaction has value. We need to think how the raw materials, intermediates and the product will be handled in a commercial plant. They influence every processing step and disposal.  

Of the three states, liquids are the easiest to handle as they can be poured, metered and pumped with ease. Solids can be weighed but their handling in the lab vs. bulk can add their own challenges especially when the solids are hazardous. Hazard and handling can be somewhat improved or reduced/eliminated if the solid can be used as a liquid (solution or melt). Dilution to improve handling lowers process productivity. Economics has to be considered.  

Reaction products, if liquid, have a hidden value. If their melting point is compatible with the process operating temperature, reaction product can replace or minimize solvent use, there by improving process productivity. Most of us overlook this simple nuance but who recognize it, know its value. 

Raw materials that are gaseous at room temperature are best handled as liquid. Their use in the laboratory as liquid is limited and safety precautions are needed for safe handling. Their use in a commercial plant can be done well if the gas is metered in as a liquid. Exotherm of such reactions can be absorbed as the liquid converts to gas. An interesting example is ammonia as liquid vs. ammonia as 35.6% solution. Productivity and process conditions are significantly different in each case. 

Solids have their own nuances and also can create challenges. If the reaction can be carried out as a melt it can minimize or eliminate solvent use and improve process productivity. However, due to volume of material to be handled and produced such opportunities are generally limited to continuous processes.  

Hazardous chemicals require extremely careful handling. Batch vs. continuous process most likely will require different handling equipment and process. What might work for a batch process might not work for continuous process and vice versa. If hazardous solid raw material can be dissolved in a solvent or suspended as a uniform slurry, their metering can be better managed and controlled. Inert thickening agents like the kind that are used in the coatings industry can be used to create a pumpable uniform slurry. This is an unconventional approach and minimizes productivity loss that can happen due to excessive solvent needed for dissolution. Concept sounds simple, but can be a challenge. Ideas like this might seem farfetched. When they work they are called innovation. 

Solids when blended to create uniform powder behave very differently due to their densities, particle size, shape, viscosity, angle of repose, mixing characteristics (5)and processing conditions including temperature etc. As discussed later, they effect equipment design and selection for a batch or a continuous process. As suggested earlier what might work for a batch process might not work for a continuous blending process. 

Intermediate reaction products, if solid can create challenges. Their solvency in a solvent of choice facilitates the process. They can be solid and will have to be handled in a manner that will maximize process productivity.  

Liquids due to their mutual miscibility or lack of it can create opportunities e.g. in separation. Lack of miscibility can be changed by using different solvents. Many do not recognize and as explained later one can capitalize on this solubility and their density differences. Different solvents can facilitate processing, improve process productivity and have financial and environmental impact. It is most productive if one additional solvent besides water can be used in the process. Disposal costs are thus limited. More than one organic solvent used in the same process add complexity and cost to the process. Experience of the chemist and chemical engineer and their ability to recognize such subtleties matter.  

Physical and Chemical Properties:

Once we know and understand different properties of chemicals, we can capitalize on their mutual behavior to create a process architecture that is economic and optimum for the needs. First time I saw physical and chemical property data details, their value did not register till I needed the information for process design and debottlenecking. They were a godsend. 

As has been discussed, physical and chemical properties are the building blocks of every process. Many of the physical and chemical properties may not be readily available. Some can be obtained from product suppliers and also retrieved from different chemical databases(too many to cite). Getting some of the mundane information e.g. solubilities, specific heat, viscosity, heat of formation etc. can be a challenge. If some of the values are not available they have to be developed. Solubilities in different solvents or different temperatures are not available from databases and they might have to be generated the old fashion way. Azeotropic behavior along with solvent miscibility/immiscibility is of values can be used to advantage.

Harnessing and creatively manipulating physical properties of solids to produce a consistent blend, that will not be prone to separation, can change the solid formulation landscape, especially for pharmaceuticals. Effort that is very different from what has been considered/tested and practiced would be needed. Some could say that it would be “impossible” to come up with a solution where separation can be minimized. However, I would say “we would be significantly challenged”. Formulators will have to think and step outside their comfort boxes. 

If we come up with a viable solution, my conjecture is that formulated products that have over trillion sales dollars per year could be impacted. Success could result in continuous formulation of many products especially pharmaceuticals (operating 7,140 hours operation per year per product per dose) would become a reality. We should see significant cost reductions, improved profitability and increased affordability. Existing equipment can be easily used. Few examples are referenced(1, 2, 3, 4)

Reaction kinetics can be manipulated to simplify design and process yields i.e. process economics. It can be of significant advantage. Raising the reaction temperature by about 10 0C, a simple quirk, doubles the reaction rate is of considerable value and works. It improves the whole process, design and economics.  

Equipment Design:

A critical element in the process design is the volume of product that needs to be produced. Product volume is the fundamental building block and a critical differentiator between a batch and a continuous process. Product costs, process economics and ROI of the investment depend on product demand. 

Combination of unit processes and unit operation make processes that produce the needed quality products. Physical and chemical properties of chemicals involved influence process design. Many books have been written on the subject. However, how different equipment and configurations can be creatively used depends on process designer’s imagination. They are difficult to write and only can be documented after their successful use to produce products. Many are considered proprietary. Volumes have been and can be written to document creative applications. Some examples (1)are discussed.  

Engineers/inventors at various equipment manufacturers, based on the needs they perceive for their customers, create and design different equipment and applications. However, the designed equipment could and does have value in other process applications that are not on their radar. Many times such uses and applications are not obvious. Engineers, do recognize their value and use them to simplify their processes. Selling application of such cross-fertilized equipment and their value internally takes out of the box thinking and sometimes skunkworks. Such innovations are considered proprietary and least documented.    

Plate and Frame heat exchangers e.g. Alfa-Laval (6)and others provide versatility of not only a heat exchanger but as a compact micro-reactor. Unknown to the suppliers we used such heat exchanger in early seventies with exceptional success. Creativity and imagination are needed to capitalize on such possibilities. Different breed of tubular heat exchangers (7)that are not used in the chemical industry are available and provide excellent possibilities of not only heat exchange but reaction space also. Such exchangers are significantly less expensive than the micro-reactors that are being tested in different laboratories and may be used in very specialized processes. Their use is ROI dependent.  

In certain applications, mostly due to tradition, high speed dispersers of high horse power are used. They pose their operating challenges. Inline dispersers (8)are economic, available and can be used. In certain applications they deliver similar results. They also provide significant operating flexibility e.g. a batch to continuous process conversion. One has to figure out their applicability and value. These along with an inline eductor can be used for dissolution and dispersion. 

As mentioned earlier, density differences of liquids can simplify processing. Value of density differences and hydraulics is of value in the design of gravity phase separators (decanters). If used thoughtfully, they can eliminate investment in exotic process controls that are generally considered a first option. I have seen decanters with fancy process controls but many become an operating bottleneck if their design is not understood by operating personnel. A decanter(9) based on specific gravity and hydraulic balance, if properly designed, is a simple and poor man’s elegant device. Most of the fancy process controllers (investment) disappears.   

Process Design:

Mass balance of every chemical reaction is important as it gives us the knowledge of what to expect. Information can be used to exploit mutual behavior of chemicals in process design, optimization, and waste disposal. Sometimes the reaction side products can pop surprises due to their toxicity and hazardous nature. They have to be dealt with. Scale up from lab to pilot plant gives us a better picture of how the process will behave chemically and physically. All of the generated information along with product volume can be readily used to commercialize a batch or a continuous process. However, many a times what works in the lab does not necessarily work in the pilot plant and scale up to a commercial plant. Changes have to be made and that is where the experience is put to test. 

In every manufacturing situation there are two kinds of processes: Batch or Continuous. Each has a well-established definition(10, 11). Routes are product volume and time dependent and there are no two ways about it. At times many forget the time element part of the continuous process. Time is an essential part of the definition. Batch processes are time interrupted. In continuous process, there is no stop and go except for the designated downtime for preventive maintenance and any production hiccups. 

There are few other very striking differences in the two routes. Since batch processes are stop and go, intermediate product after every step generally by force of habit is sampled, tested and the process corrected if out of spec. Intermediate sampling is an addiction and extends batch processing time. Stoichiometry deviation in reactive and formulation batch processes can happen if the operating instructions are not followed precisely. This generally results in lower overall yield and a financial loss. Such processes producing quality by analysis could also be called quality by aggravation (QbA).  

Stoichiometry in continuous reactive as well as formulation processes cannot deviate from design parameters. Designed process has to produce expected product quality every instant of the operating time. Compared to batch processes continuous processes are not at all forgiving to any deviations. Excursions outside the specifications can be an economic disaster. Uniform distribution of components in formulated products is very critical especially in formulations. Thus as stated earlier complete command is a must. Product quality has to be built in the process design and cannot be tested in.

Companies have to select the process to be used based on their business, short and long-term strategy, competition and expected return. Since each process, batch or continuous, is an independent route to produce the product, scale and method of execution of same unit process and unit operation can be different. Engineers and chemists are creative and do their best. We have to recognize that the equipment selected for a batch process can be retrofitted to produce many other products. However, such luxury does not exist for any continuous process as their design is product specific.   

Process controls based on process logic can make some changes within the designed limits in the stoichiometry but still the resulting product cannot deviate outside the product quality expectations. Today’s process controllers and logic are extremely robust and sophisticated to deliver the designed quality product. As said earlier if the product volume is there, continuous processes are generally method of choice. 

Batch and continuous processes have their own nuances of product supply and inventory. How they are handled and managed impact cash flow and cannot be overlooked. Manufacturing folks at times have to simultaneously wear many hats: manufacturing, accounting, marketing and purchasing.   

It is also important for the creators and the designers of process to document their thinking, rationale and the design basis. This includes mass and heat balance, equipment selection rationale and design calculations etc. It might be considered a mundane task but is a gift for the upcoming engineers and chemists. They would know how, what and the why of the design. This information comes in handy for trouble shooting, debottlenecking, filings and discussion with any regulatory authority. First time I had to document my design basis, rationale and calculations, it seemed to be a pointless exercise. However, was thankful for it being available when I needed the information for the task at hand and later work by others. 

In the annals of chemistry and chemical engineering there are many cases where equipment, physical and chemical properties have been married to create very simple and elegant designs and simplify existing batch and continuous processes. Chemists and chemical engineers at every company are the innovators and creators (12), and as stated earlier are the Picasso, the Michelangelo, the Zaha Hadid or the Gaudí or other artisansof the most innovative technologies and economic processes. Imagination and creativity are the two gifts they have and exploit. We have to let them do the best they do.     

Girish Malhotra, PE
EPCOT International 
  1. Malhotra, Girish: Chemical Process Simplification: Improving Productivity and Sustainability, John Wiley & Sons, February 2011 
  2. Malhotra, Girish: Chapter 4, Simplified Process Development and Commercialization” in “ Quality by Design-Putting Theory into Practice, co-published by Parenteral Drug Association and DHI Publishing© February 2011
  3. Malhotra, Girish: Focus on Physical Properties To Improve Processes: Chemical Engineering, Vol. 119 No. 4 April 2012, pgs 63-66
  4. Malhotra, Girish: Process Simplification and The Art of Exploiting Physical Properties, Profitability through Simplicity, March 10, 2017
  5. Tekchandaney, J. Material Properties Affecting Solids Blending and Blender Selection, August 22, 2009 Accessed October 8, 2018
  6. Alfa-Laval
  7. Process Technology
  8. Ross Inline dispersers
  9. McCabe W.L. & Smith J. C., Unit Operations of Chemical Engineering, McGraw-Hill Book Company 1967, page 40
  10. Batch Production: https://bit.ly/2ptp0kS
  11. Continuous Production:https://bit.ly/2qtSYY6https://bit.ly/2POmN3Ghttps://bit.ly/2qAyc9f
  12. Malhotra, Girish: Pharma’s future is putting innovations in the hands of innovators, August 23, 2018

Thursday, July 20, 2017

Batch, Continuous or "Fake/False" Continuous Processes in Pharmaceutical Manufacturing


Use of “Fake and/or False” in our vocabulary has become very pervasive since 2016. I thought it would be useful and helpful if we re-visit definitions of Batch and Continuous production processes and try to see do either of them fit in the realm of False or Fake “B or C” process. My observations are based on my education, experiences in chemistry and chemical engineering and the prevailing practices established more than 100 years ago. They are also based on actual process design and development, scale up of developed processes and management of manufacturing processes and operations in fine/specialty chemicals, coatings, resins that were produced using organic chemicals. Many of the products were produced by reacting chemicals and others were formulated by blending different chemicals.

In recent months certain pharmaceutical processes have been labeled as continuous process but no process information has been shared. However, based on public information about the products their viability of being operated as a continuous process is extremely doubtful. Additional details are shared later.

Established batch and continuous process definitions and examples are reviewed after a brief overview of what chemical engineers are taught. I do not want to go in details but the following are part of the Ch.E. curriculum.  

Fundamentals taught in Chemical Engineering:

Chemical engineers are taught that every process should be safe, sustainable, and economic and should produce quality product first time and all the time. If a product has to be reworked or its stoichiometry has to be adjusted during the process to produce a quality product, its cost goes up and the profitability of the company is lowered.

It is well known and practiced in every manufacturing industry that the market size demand influences the type of process used. Irrespective of the process used product quality is a must for the market success of every product. These expectations are most stringent for the pharmaceuticals as they influence human life.

Chemical reactive processes are called Unit Processes (1) that produce a product that could be the final saleable product or could be an intermediate for another reactive or formulated product. Unit operations (2) involve a physical change or chemical transformation that are used in the chemical and allied industry to facilitate unit processes to produce the desired products. The combination of these makes a process and depending on demand it could be a batch or continuous process. 

McGraw-Hill has published series (3) of books that cover unit processes, unit operations and the economic considerations that allow chemical engineers and chemists to develop, design and commercialize processes that are economic and profitable to any individual or company. Besides these books there are many other books that have been written on the subject. Excellent books have been written about process control methods and strategies (4)

Most of these books have been written by what I would call “Hall of Famers” of Chemical Engineering and are considered Bibles of Chemical Engineering profession. None of these books are recommended or sponsored. There is no affiliation or financial relationship with the author.

Batch production:

Wikipedia’s (5) definition for batch production: Batch production is a technique used in manufacturing, in which the object in question is created stage by stage over a series of workstations (steps), and different batches of product/s are made. Batch production is most common in bakeries and in the manufacture of sports shoes, specialty/fine chemicals, resins, pharmaceutical ingredients (APIs), purifying water, inks, paints and adhesives. There are other formulated products and most prominent are finished pharmaceutical drug dosages.    
Batch production processes generally require much lower investment and have an advantage because several products can be produced in the same equipment. However, if the same equipment is to be used for different products, productivity will be significantly lower (6) compared to a process where the equipment is dedicated to produce a single product. If different products are to be produced in the same equipment, cleanliness becomes critical, especially for the APIs and their formulations. Idle (down) time can be high. Down time in the pharmaceutical industry is extremely high (7).  
For the pharmaceutical industry batch processes are the main stay in the manufacture of active ingredients (API) and their formulations. This is due to two inherent reasons. Micrograms to milligrams of API are needed in every dose. One kilogram of an active produces ONE million tablets of one milligram each. Thus, not a large quantity of the API is needed to satisfy the need. Table 1 is an illustration of the needed API and potential production methods for different dosages and number of patients. Additional analysis (8) is available elsewhere.

Dose, mg
Patients    Millions
API Kilograms needed/ year @ one tablet per day per year
API Production
Preferred Process Type
Number of plants
1
500
182,500
Batch
One or More
200
0.1
7,300
Batch
One
10
100
365,000
Batch
One or More

100
50
1,825,000
Batch or Continuous
Could be a single continuous plant but most likely batch
500
20
3,650,000
Continuous

Could be a single continuous plant but generally batch due to multiple sites

Table 1: Typical API need, Number of Patients and API Production Process
Process economics, chemistry and execution method will determine type of process used. Typical available hours for production at any plant are about 8,400 (24x7x50) hours per year. How many of these available hours are used for the production of a single product define the production process. If less than 8,400 hours are used to produce a product such process according to the established norms (5) will be a batch process. This holds true for API production and their formulations.
Table 2 is an illustration of how many hours per year are needed to produce at @200,000 tablets per hour at different doses. Production equipment of higher tableting rates are commercial and available. It is most likely most of the products would be formulated using batch processes even when they could be operated continuously.     

Dose, mg
Patients Millions
Tablets Used per day
Tablets, Millions/ year
Run Time Needed, hours @200,000 tablets/hr.
Number of plants
operating 7,140 hours per year
Preferred Formulation Process
1
50
1
18,250
91,250
13
Continuous but will be multiple batch plants
10
20
2
14,600
73,000
10
Continuous but will be multiple batch plants
100
15
3
16,425
82,125
12
Continuous but will be multiple batch plants
500
10
4
14,600
73,000
10
Continuous but will be multiple batch plants
200
0.1
1
36.5
183
1 (Run time less than 200 hours
BATCH ONLY
Table 2: Tablets Needed, Tablet Run time, Number of Plants and Patients Served
Continuous production:

The definition of continuous (9) production has been long established. Continuous usually means operating 24 hours per day, seven days per week with infrequent maintenance shutdowns, such as semi-annual or annual. Time could be allocated for unexpected shutdowns. Any process that does not meet the defined and established definition and is operated fewer hours than the established definition would be difficult to be justified as a continuous process. Excellent examples of continuous process are Earth’s rotation and our heartbeat. Can we imagine “stop and go” movement of earth and human heart? 

Throughout the pharma landscape most likely there are ten or less APIs that are being produced by continuous processes. There are additional APIs that could be produced continuously (10) but effort is needed to develop and commercialize such processes. Different business model would be needed. Alternate business model and consolidation can convert batch processes to continuous processes. There is a downside of the continuous processes. It will result in consolidation of operations especially among the contract API producers and formulators.

McNeil, a Johnson and Johnson subsidiary, due to the formulation volume of Tylenol could have built a continuous process but they did not, a missed opportunity. It seems that chemical engineers and chemists at some companies forgotten FRUGAL SCIENCE and FRUGAL ENGINEERING.


Fake/False Continuous processes:

In the current pharmaceutical landscape, processes that are in reality batch processes are being called continuous by the chemical engineers working in public and private sectors. We all need to understand and recognize that if multiple products can be processed in the same calendar year in the same equipment by re-arranging the reactive chemistry or the formulations, their processes would not be called “continuous manufacturing”. Any process that has a wide spot in the manufacturing line [material is held for any time period], the process is a batch process. Processing step before such hold can be called by any name but if it is different from established definition, we have are making fun of science and engineering.

FDA (11) does not have an established definition and I am told one would be forthcoming. I wonder how different it would be from what is established and practiced methods.  Even the press (12) has chimed in. Numerous articles have been written that include “continuous manufacturing” but no one has put forth its definition or names of the product or their production rates. I am sure many, me included, want to see the proof. I am sure many of us remember movie Jerry Maguire (13).

API Example:

Analyzing Table 1, we have an example of a drug that has 100,000 patients. They have to take 200 mg dose every day of the year. Total API needed is about 7,300 Kg. per year. This product would and should be produced using a batch process in the available equipment. If each batch reaction produced about 250 kilos per batch and about 30 batches per year would be needed. If each batch took 30 hours per batch all of the API would be produced in about eight weeks. If they campaigned the whole production for first two months of every year, this would not make their process a continuous process. If this campaign run was called a “continuous process” then it would be an incorrect characterization and I will label this process “fake/false continuous process”.  

Formulation Example:

If the example of API above was to be formulated and tableted, the product can be produced at single plant in less than 200 hours at 200,000 tablets per hour. However, if the tableting were done at 10,000 tablets per hour, it would take them six months to produce the total demand. It still does not make the process continuous, as the equipment would be sitting idle for six months every year. It would be a wasted investment earning no return if every reader of this post had to invest his or her own money. Again if the process is called a continuous process, it again would be an incorrect characterization and I will label this process “fake/false continuous process”.

Vertex (8) has claimed to have a continuous process for their cystic fibrosis (CF) drug. With less than 80,000 patients worldwide, they do not have large enough global patient (~80,000) base for all of their CF drugs and cannot operate their equipment for 8,400 hours per year per drug. Similar situation exists for Janssen Pharma drug Prezista.

To me, an incorrect characterization of established definitions seems to have become a new fashion especially in the pharma landscape. Is it because the US FDA is mentioning continuous manufacturing in their communications and the industry wants to look good by calling a naturally batch process as a “continuous process”? Thus, if we accept an incorrect definition then we should be also ready to accept 2+2=6, Sun can rise from the West and a mammal can be half pregnant (my apologies to all readers). If that were the case basic laws of science, math and anatomy would be defied.
Quality Assurance in Batch and Continuous Processes:
Meeting quality standards in batch as well as continuous processes have different rigors. Command of the processes is a must whether it is a batch or a continuous process. If command and understanding of the processing steps are lacking, invariably there could be a batch-to-batch and/or a lot-to-lot quality variation. Efforts to rework or bring the material to quality can and often results in waste i.e. higher product costs.
In batch processes due to their stop and go nature quality can be sometimes managed and the process adjusted to achieve the established quality benchmarks. Thus an absolute command of the batch process is less stressful but still is necessary. Batch processes are based on in-process quality checks and adjustments. This practice extends cycle time and adds to inventory [raw material, in-process, work in process and finished goods] challenges. If the batch process cannot be adjusted to correct process deviation, significant waste can result. In the simplest terms, batch processes have economic value for products that do not require continuous production but their quality testing can be an aggravation. Batch process = quality by aggravation (QbA) unless the process repeatability is strictly controlled.  

Compared to batch processes, continuous processes have much higher process control demand. Since the process is running with minimal/no stop time, it is extremely critical that process operating parameters do not deviate outside the established process operating control limits. If process deviates outside the established control limits, significant quantities of waste and financial loss can result. Continuous processes demand that the quality be established through robust process design when the process is developed, designed and commercialized. This would be a case of quality by desire (QbD).

I am sure the debate on what is a continuous or a fake/false continuous process will go on till the economic realities of investment that have been well established are understood by most. Chemical engineers and Chemists are taught everything, values and virtues, of batch and continuous processes there is to know about such processes but one thing is sure unless one has not justified, developed, designed or commercialized a process, it is difficult to discern value of the developed process. I know no investment would be made for namesake unless it can be justified and meets established norms of the science, economics and engineering.

As I said earlier a batch process cannot be continuous and vise versa. If we accept it otherwise then we have a case of “false/fake” science, engineering, economics and human intelligence.  


Girish Malhotra, PE
EPCOT International

  1. Shreve, R. Norris: Unit Process In Chemical Processing, Ind. Eng. Chem.195446 (4), pp. 672–672
  2. Unit Operation, https://en.wikipedia.org/wiki/Unit_operation, Accessed July 11, 2017
  3. McGraw Hill Chemical engineering series, https://www.librarything.com/tag/McGraw+Hill+Chemical+engineering+series, Accessed July 6, 2017
  4. Chemical process control, https://www.librarything.com/subject/Chemical+process+control, Accessed July 6, 2017
  5. Batch Production Wikipedia, https://en.wikipedia.org/wiki/Batch_production Accessed July 6, 2017
  6. Malhotra, Girish: Square Plug In A Round Hole: Does This Scenario Exist in Pharmaceuticals? Profitability through Simplicity, August 17, 2010 Accessed July 11, 2017
  7. Benchmarking Shows Need to Improve Uptime, Capacity Utilization, Pharmaceutical Manufacturing, Sep 20, 2007 Accessed July 7, 2017
  8. Malhotra, Girish: A Blueprint for Improved Pharma Competitiveness, Contract Pharma, September 2014, pp. 46-49
  9. Continuous Production, https://en.wikipedia.org/wiki/Continuous production, Accessed July 14, 2017
  10. Malhotra, Girish: Strategies for Improving Batch or Creating Continuous Active Pharmaceutical Ingredients Manufacturing Processes, Profitability through Simplicity, March 20, 2017, Accessed July 17, 2017
  11. Drug Making Email exchange with Dr. Janet Woodcock, FDA July 13, 2016
  12. Breaks Away From Its Old Ways, The Wall Street Journal, February 8, 2015, Accessed July 17, 2017
  13. Jerry Maguire, Accessed July 18, 2017