The Role of Process Piping in Manufacturing Efficiency

pharmaceutical-process-piping

Pipe systems are conduits for liquids, gases and solid substances all through industrial plants, with the primary purpose of carrying raw materials, finished products and other utilities like steam, water or cleaning fluids from one place to another. Used across industries, sanitary and otherwise, they are generally considered to be a comprehensive, interconnected network including all pipes and associated components like connectors, pumps, valves and a lot more.

What is the role of pharmaceutical process piping?

You may have equipped your pharmaceutical or biotech facility with the most cutting-edge tanks and machines but without high quality pharmaceutical process piping, all of those expensive CAPEX investments are worthless. After all, your APIs and excipients are only worthwhile when they are carried through the complex network of your plant in the process of preparing your final product.

Pharmaceutical piping is critical to your manufacturing plant’s operations. While similar to process piping in other industries, pharmaceutical process piping has its own set of functions and design and engineering specifications. In terms of sanitation and quality, pharmaceutical piping has extremely stringent requirements. And then there are also tremendous gains in efficiency that good pharmaceutical piping design can give you. In a world where your competitors are neck and neck with you to bring the next big drug to the market, it’s always smart to invest in the highest quality infrastructure so that you can compete with them on more than just price.

Why is having quality process piping so critical?

Process piping in pharma and biotech is extremely critical to ensure products move from one place to another safely, quickly and efficiently. Not just because of stringent pharmaceutical piping specifications, but also because this extensive network interacts with so many elements in your manufacturing process.

Pharmaceutical process piping comes in contact with raw materials and final products, so you want to make sure it doesn’t pose any contamination risks or affect the integrity of your end product in any other way. In order to maintain this high level of sterility, the multiple bends and curves in your pipes of various diameters need thorough cleaning at regular intervals to make sure residue from previous production batches, cell debris, cleaning agents or any other substance are cleared.

Just as the case is with process vessels and machines, your pharmaceutical piping must also be designed to withstand fairly high temperatures and pressures. Plus, the risk of corrosion from pipe materials must be eliminated. As must any other potential unforeseen blockages – something the video boroscopes in TSA process piping systems help you monitor regularly.

Sanitary standards in pharma are exceedingly high, as they should be. So we’re sure you don’t want to compromise on any of the above factors, do you? But then, additionally, you also want to optimise your pharmaceutical piping design for process efficiency. Poor pharmaceutical piping design can have extreme consequences, but carefully considered piping has the potential to radically enhance the productivity of your plant.

Your pharmaceutical process piping can be designed with care, with precision, in such a way that minimises waste and cycle times, maximises throughput and yield, and ensures repeatability and reliability. In short, your pharmaceutical piping can be customised to optimise the flow of people, materials and information.

Pharmaceutical piping specifications

As with all other aspects of pharmaceutical production, pharmaceutical process piping also has its fair share of regulatory standards and specifications to comply with. For starters, irrespective of the country in which you are producing or installing your process piping, complete qualification and validation is a non-negotiable.

Pharmaceutical piping specifications also include complete QA/QC procedures which are well-defined and approved by third parties. Finally, internationally recognised standards, like current Good Manufacturing Practices (cGMP), American Society of Mechanical Engineers (ASME) Bioprocessing Equipment (BPE) standards, and 3-A give your customers the confidence that your piping can serve their needs in the best way possible.

At TSA, all process piping complies with cGMP, 3-A, and ASME-BPE standards.

Pharmaceutical piping design

Considering the scale of pharmaceutical piping, building the entire piping network in your plant is an expensive affair, second only to your investment in sophisticated equipment. This is why you want to make sure that even before you begin to install piping, you have a solid design which will assure you of quality, safety and efficiency.

Every pharmaceutical process piping system is uniquely tailored to its application and site. Given the highly specific nature of each piping system, there are some important things to consider while in the design process:

  • Limitations and opportunities in the physical space
  • Access for maintenance
  • Integrated CIP and SIP functionalities
  • Drainage points
  • Temperature of the substances being transported
  • Pressure at which the liquid or gaseous substance flows through the piping system
  • Viscosity of the products being transported
  • Product’s corrosiveness
  • Desired flow rate

Properly designed and engineered systems are not just a boon, but a necessity in the pharma and biotech industries. They allow manufacturers to produce consistent, high quality pharmaceutical preparations. This is all the more reason to ensure your process piping is a good investment.

This involves a stress analysis – governed by international regulatory agencies – in the design phase to make sure that the pharmaceutical piping, loads and supports are appropriately placed so that you don’t shoot over allowable pipe stress under diverse conditions like pressure testing and operating loads.

Other things to keep in mind about your pharmaceutical piping

There are a few other things to keep in mind about the importance of the role of pharmaceutical process piping to ensure efficiency in your manufacturing plant:

Weather and climatic conditions

The external environment naturally has an effect on pharmaceutical piping systems’ performance. A pipe transporting fluids heated to extremely high temperatures in a location with a cold climate risks bursting or fracturing. Meanwhile, transporting cold substances in pipes during hot weather can have adverse impacts on the piping system’s strength. Some of the factors mentioned below will address this concern.

Maintenance

All pharmaceutical process piping must be fully cleanable, sterilisable and drainable. It cannot afford to have any dead legs. Surfaces, especially the inside ones which come into contact with raw materials and final products, must be electropolished and comply with industry standards. At TSA, our orbitally welded piping systems available with CIP/SIP integrations tackle all these concerns.

Material of Construction

Stainless steel 316L is the best metal out there to make sure your pipes are strong, stable, easily cleanable, and resistant to corrosion that might affect your raw materials and final product. However correct choice of material has to be taken in to consideration with respect to the products being transferred

Pipe connections must be leak proof

Leaks not only compromise the safety of your personnel and the larger environment in which you are situated, but they also allow contaminants to find their way into your system. This is an absolute no-no.

Pipe supports

Your pharmaceutical process piping system must be supported adequately while also ensuring that the combined weight of the pipes, supports and other allied products does not cause the line to sag. You also want to design them in such a way that permits expansion and contraction of the pipes under varied temperature and pressure conditions.

Pipe insulation

As mentioned in the first point here, your piping should be able to handle the climate of the region your plant is situated in. Insulation is a good solution for this problem. Good insulating materials have properties like being vermin-proof, having high insulation value, corrosion-resistance and long life.

Sizing

Pipe sizing is of utmost important. This will help the system to run to optimum capacity as wrongly designed pipe sizes may cause disruption in production. The correct sizing in turn ensures right quantity at the time of productions

At TSA, all process piping is of the highest quality, customisable to your specific site and application needs. They comply with internationally-recognised standards and will ensure a smooth process for you from design and fabrication to installation, operation and maintenance. If you’re looking to install or upgrade your pharmaceutical process piping, get in touch with us now. We love solving your toughest challenges.


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Hetal Panchal is the Vice President in Operations department of TSA Process Equipments (A Thermax Group Company) since 1 s t October 2012.

Holding a qualification in Production Engineering and 28 years of industry experience, he specializes in designing advanced equipment for the pharmaceutical sector. His expertise lies in optimizing production lines, improving efficiency, and ensuring compliance with regulatory standards.
Focused on innovation, he has developed systems that enhances productivity, minimizes downtime, and maintains product quality. Staying current with technological trends, they contribute to ongoing improvements in the industry.
His extensive experience has helped identify opportunities for innovation, streamlining operations and reducing costs. Through his specialized knowledge, more efficient manufacturing processes and higher-quality outputs in pharmaceutical production are delivered.

B.C. Mahesh is the Chairperson of TSA Process Equipment Pvt. Ltd. since Feb 2024.

B.C. Mahesh became a member of the Executive Council in August 2013. He is responsible for the Industrial Product Business (IPB), which consists of Process Heating, Absorption Cooling & Heating Solutions, Water and Waste Solutions, Air Pollution Control, Steam Engineering, Channel Business Group, International Business Group, and Enterprise Sales businesses.
As part of IPB, he also oversees the following wholly-owned subsidiaries
of Thermax – Danstoker, PT Thermax International Indonesia and Rifox.Mahesh joined Thermax as a graduate trainee in 1988 and handled the Materials function for various businesses, including global sourcing, till 1996.
He moved to the Power division(P&ES) and grew to the position of Sales Head and subsequently Head of Projects. He took over as the Head of the SBU for Medium Power Plants in 2009 and finally as Head of Power business in 2012.
Mahesh has worked with Thermax for over 30 years in many functions such as manufacturing, supply chain, sales and marketing, and project management, and has played a significant role in the strategy, expansion and diversification of the Power business.Mahesh completed his Mechanical Engineering from the Visvesvaraya Regional College of Engineering, Nagpur in 1988.

Vishal Mehra is the Director of TSA Process Equipment Pvt. Ltd. since Feb 2024.

Mr. Vishal Mehra is currently serving as the Strategic Business Unit Head for Water & Waste Solutions (WWS) at Thermax Limited. Additionally, he holds a directorial position at TSA Process Equipment, which is known for its expertise in ultra-pure and high-purity water technologies and was recently acquired by Thermax.With over 22 years of experience in the industry, Mr. Mehra’s professional focus includes water management solutions, advanced technology development, and business strategy.
His areas of interest encompass cutting-edge technology, growth strategies, organizational effectiveness, and development.
Mr. Mehra is well qualified in business management and strategy transformation, having completed the Senior Executive Program in Business Management and Strategy Transformation from London Business School. This advanced education supports his extensive experience and expertise in the field.

Sandeep Deshpande has been the Director of TSA Process Equipments Pvt. Ltd. since February 2024.

Currently, he serves as the Head of Corporate Finance and the Industrial Product Group at Thermax Limited. With over 21 years of experience in finance, he has developed expertise in financial consolidation, planning, reporting, costing, accounting, controlling and financial modeling.
Currently, he serves as the Head of Corporate Finance and the Industrial Product Group at Thermax Limited. With over 21 years of experience in finance, he has developed expertise in financial consolidation, planning, reporting, costing, accounting, controlling and financial modeling.
Sandeep is a qualified Cost Accountant Company Secretary, and holds a diploma in IFRS and an advanced diploma in financial management from XLRI. He has extensive experience in financial operations, including financial planning, MIS, budgeting, controlling, audits, and cash flow management. His expertise also spans financial reporting, consolidation, mergers and acquisitions, due diligence, business restructuring, and implementing Internal Financial Control (IFC) and Enterprise Risk Management (ERM). Additionally, Sandeep has hands-on experience with Oracle systems, automation, digitization, and business analytics. He is passionate about driving good governance, improving financial reporting, and leveraging automation and digitization to enhance business analytics.

Rajiv Parikh is the COO of TSA Process Equipments (A Thermax Group Company) since April 2024.

Rajiv is a highly accomplished professional with extensive experience in the pharmaceutical and FMCG sectors, specializing in high-purity and process vessels. He played a key role in establishing TSA Process Equipments Pvt. Ltd., driving its growth and success. His deep technical expertise, combined with a strong understanding of client needs, has enabled him to deliver innovative solutions to complex industry challenges.

Throughout his career, Rajiv has excelled in leadership and sales, consistently launching cutting-edge products that have positively impacted the market. His ability to build lasting client relationships and offer tailored solutions has earned him a reputation as a trusted industry leader.

With a background in Mechanical Engineering, Rajiv blends technical proficiency with strategic vision. His contributions have shaped industry standards and positioned him as a key influencer in the pharmaceutical and FMCG sectors.

Apurva Shah is the CEO of TSA Process Equipments (A Thermax Group Company) since April 2024.

With a career spanning over 24 years, Apurva is the visionary CEO of TSA Process Equipments, where he has led the company to new heights in the High Purity & process equipment industry. A graduate in Mechanical Engineering from Mumbai University, followed by an MBA in Business Management from NMIMS, He brings a strong technical foundation combined with a sharp strategic mindset.

His expertise lies in formulating and executing strategies that drive growth and operational efficiency. Over the years, he has cultivated a deep understanding of market dynamics, positioning TSA Process Equipments for continued success in a competitive landscape.

Outside of his professional pursuits. He is an avid reader, with a particular interest in fiction novels, which fuel his creativity and broaden his perspective.