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PDA releases contamination control strategy report

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Technical Report 90: Contamination Control Strategy Development has been released by the Parenteral Drug Association (PDA).

PDA releases contamination control strategy report

The Parenteral Drug Association (PDA)’s long-awaited Technical Report 90: Contamination Control Strategy Development in Pharmaceutical Manufacturing is now available.

 

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This report addresses the key factors shaping pharmaceutical formulation, including regulation, QC and analysis.

Access the full report now to discover the techniques, tools and innovations that are transforming pharmaceutical formulation, and learn how to position your organisation for long-term success.

What you’ll discover:

  • Key trends shaping the pharmaceutical formulation sector
  • Innovations leading progress in pharmaceutical formulation and how senior professionals can harness their benefits
  • Considerations and best practices when utilising QbD during formulation of oral solid dosage forms
  • And more!

Don’t miss your chance to access this exclusive report ! Access now – it’s free

Developing a contamination control strategy (CCS)

According to the PDA, contamination control measures have been a core element of good manufacturing practices in pharmaceutical drug manufacturing for decades.

These control measures are a collection of generic practices developed separately and applied without clear consideration for their interdependence, the organisation noted.

Key features of the PDA TR 90 report

The document addresses the evolution of contamination control principles towards a holistic approach. This means practices are designed to work together to achieve proactive contamination control and are evaluated for their collective effectiveness. Therefore, contamination control measures are tailored to the specific risks around each individual process.

The PDA’s report focuses on contamination control practices against microbial and other adventitious agents, endotoxins, and foreign particulate matter in the manufacture of sterile drugs, low bioburden drug substances, and some nonsterile drugs that are vulnerable to contamination.

The document has 14 sections and five appendices. Within the main sections, the areas covered include:

  • Elements of a CSS
  • Considerations on quality risk management (QRM) and quality control (QC)
  • Design and control considerations for facilities, equipment, personnel, cleaning and waste procedures
  • Raw materials and navigating contamination risk
  • Considerations for product container closure
  • Environmental monitoring

The appendices in the contamination control strategy report also cover microbial impact assessment and contamination control case studies.

Dr Madina Karimova, Quality Assurance Manager at Sanofi shared her opinion on PDA’s TR 90 report, highlighting parts she found valuable.

Ultimately, the new CSS document can help the pharmaceutical manufacturing sector to develop and implement a successful CCS.

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