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Process Pharma Technologies

Specialized process needs for biopharma 

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Process Pharma is a multifaceted supplier of industrial bioprocess ingredients tailored to specific requirements for process consumables.  We specialize in providing complete systems including:

High yield precipitation and separation methods, Microfiltration & Ultrafiltration, NANO & RO filtration, Ion Exchange and ligan or hydrophobic based detergent sequestering resins.


Applications for purification technologies and validated components for your process, validation services for viral inactivation and removal technologies.


It is through this practical knowledge that we understand your special filtration and business needs. Our understanding of the business and the processes guarantee the best solution for your specific needs and budget. Contact us today!

ABOUT

 

We have successfully delivered and implemented complete technology solutions for projects across a wide range of industries worldwide. With a strong foundation in biopharmaceutical applications and the production of high-purity materials, we are committed to identifying the ideal products for your specific needs — at the best value and in full compliance with your validation requirements.

As a single-source supplier, we cover your entire value chain — from active ingredients and consumables to advanced technologies for fermentation, purification, and separation of biological proteins.

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Ongoing projects not limited to:

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  • Viral inactivation for immunoglobulin preparations.

  • Novel pharmaceuticals: pegylated immunoglobulins.

  • Viral removal technologies in biological products.

  • High purity protein purification storage systems and disposable containers formulated for proteins.

  • Specialty chromatography resins and filters for biological applications.

  • Separation of biological proteins, centrifugation and filtration processes.

  • Plasma derived products, process integration.

>130

Customers

>9

Countries

Our Services

1

Process Engineering

We support you throughout every stage of your pharmaceutical process and production lifecycle. From designing your facilities and processes to procuring, commissioning, and qualifying production equipment — and optimizing existing operations — we are your reliable and experienced partner.

Our team consists of seasoned specialists with extensive experience in the design, operation, and commissioning of sterile filling lines, isolators, and freeze dryers.

Our process engineering includes

Human Plasma Fractionation, protein purification, aseptic processing of APIs and redundant systems for continued non-stopping processes.

2

Engineering Services

We offer comprehensive engineering support from the initial feasibility study through to handover for routine operation — including employee training.

Our services include:

  • Process design, including material and personnel flow optimization

  • Development of User Requirement Specifications (URS) in compliance with current GxP guidelines

  • Project management, including claim and change control

  • Construction management and coordination of commissioning activities

  • Execution greenfield projects 

3

Total Expertise

We bring deep expertise across critical areas of biopharmaceutical manufacturing support

Our capabilities include:

  • Design of production processes for bulk manufacturing, fill & finish, and lyophilization

  • Technology transfer from R&D to commercial production (scale-up and scale-out)

  • Technology transfer to new manufacturing sites

  • Change control management related to tech transfer activities

  • Process optimization for fill & finish, bulk production, and lyophilization

  • Definition and design of filtration processes, including point-of-fill filtration

  • Development of regulatory submission strategies and concepts

Expert Services in Human Plasma Processing

The Critical Role of Human Blood in Modern Medicine

Human blood is indispensable not only for transfusions but also for the development of life-saving therapies. Plasma-derived medicinal products—extracted from donated blood—are essential in treating a wide range of conditions, from hemophilia and immune deficiencies to viral pandemics. Plasma derived therapies are in high demand, and their production involves a series of highly specialized, tightly controlled processes. Precision across the entire value chain ensures that every drop of plasma is used to its fullest therapeutic potential.

A Growing Market with Rising Demands

The global demand for plasma derivatives continues to rise, driven by advancements in medical technology and an increasing prevalence of rare and chronic diseases. While recombinant techniques—those using genetic engineering—have reduced reliance on human plasma for some therapies, many vital proteins such as albumin, immunoglobulins, and coagulation factors are still best sourced from plasma. Concurrently, improvements in plasma fractionation technology have boosted the yield and purity of these valuable components.

At the same time, the growing incidence of blood clotting disorders, rare genetic diseases, and immune-related conditions further underscores the importance of a stable and scalable plasma supply. Meeting this demand requires not only raw materials, but also sophisticated, high-yield processes that minimize waste and ensure patient safety.

From Donation to Therapy: A Complex Journey

Before plasma can become a safe and effective medication, it must undergo multiple rigorous processing stages. Typically delivered frozen, donated plasma is first thawed, then fractionated, purified, formulated, and finally filled, freeze-dried, pasteurized, and inspected—depending on the final product requirements.

Given the complexity of these operations and the scarcity of human plasma, precision and process control are vital. Every milliliter lost during production not only impacts cost but also represents a missed opportunity to treat a patient in need. For this reason, manufacturers prioritize high recovery rates, process flexibility, and consistently high product quality.

Thawing and Fractionation: Precision at the Core

The journey begins with thawing frozen plasma, typically supplied in large bags or bottles sourced from multiple donors. To preserve the integrity of sensitive proteins, thawing must occur gradually in specialized systems designed to gently mix and warm the material under low shear conditions.

Once thawed, the plasma undergoes fractionation—where it is separated into components like albumin, immunoglobulins, fibrinogen, and other coagulation factors. This process relies on a series of precise filtration steps, which isolate proteins based on size, charge, and affinity. Such complex processing demands advanced, scalable equipment capable of delivering stable, efficient results at industrial volumes.

Integrated Systems for High-Quality Demand Expert Services

Process Pharma Technologies provides All-in-one, fully automated solutions from a single provider help ensure continuous monitoring, seamless integration, and control of critical process parameters. Each phase of the process of plasma fraction process requires rigorous measures to remove impurities and inactivate viruses using chemical or heat-based methods.​

CONTACT

Process Pharma Technologies offers a comprehensive range of solutions for the biochemical, pharmaceutical, and biopharmaceutical industries. We supply high-quality products tailored to meet sanitary, high-purity, and industrial processing requirements — with a strong focus on critical protein purification and the continuous supply of essential materials to ensure reliable process performance.

We invite you to consider us for your next project. At Process Pharma Technologies, we pride ourselves on delivering exceptional service, competitive pricing, and fast, reliable delivery.

Inquiries

For inquiries, questions or commendations, please fill out the following form:

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Offices

PropharmatecHead Office

500 Supor Blvd. Bldg. 1

Harrison, NJ 07029

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webcontact@propharmatec.com

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New distributor serving South East Coast

1200 Woodruff Rd

Greenville SC, 29607 

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© 2025 Process Pharma Technologies

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