The Means to Monitor Chemical Migration - Pharmaceutical Technology

Latest Issue
PharmTech

Latest Issue
PharmTech Europe

The Means to Monitor Chemical Migration
Industry associations will soon provide new recommendations about extractables and leachables.


Pharmaceutical Technology
Volume 35, Issue 6, pp. 40-42

Good manufacturing practice and FDA regulations require pharmaceutical companies to know their production processes. Understanding the chemicals that potentially could migrate into final products is crucial, particularly for companies that incorporate single-use equipment within their facilities. Manufacturers need to identify which chemicals could migrate and quantify the likelihood of this migration. A forthcoming Parenteral Drug Association (PDA) technical report that recommends a risk-based approach, and pending safety and analytical thresholds from the Product Quality Research Institute (PQRI), will help drugmakers develop appropriate extractables-and-leachables strategies.

The PQRI document


IMAGE: ANDERSEN ROSS, LAWRENCE LAWRY, GETTY MAGES. COMPOSITE: DAN WARD
In 2006, PQRI published recommendations to help drugmakers develop safety thresholds for extractables and leachables in orally inhaled and nasal drug products (OINDP). The group is currently at work on a companion document that will address extractables and leachables in parenteral and ophthalmic drug products (PODP). The new document will be submitted to the PQRI Steering Committee in 2012, according to Diane Paskiet, chair of PQRI's leachables and extractables PODP working group.

The PQRI working group writing the document includes industry experts and representatives of the US Pharmacopeia, FDA, and HealthCanada. The group is divided into a chemistry team, which will discuss how to conduct extractables studies, and a toxicology team, which will provide advice about evaluating chemicals' safety.

PQRI will submit the final recommendations document to FDA. The document is intended to demonstrate best practices for the evaluation and qualification of leachables in parenteral and ophthalmic drug products. These practices have been extrapolated from the OINDP recommendations, and future documents could potentially address other dosage forms or routes of administration, says Paskiet.

The focus of the PODP document is to demonstrate how to conduct controlled extraction studies to understand the chemistry of the materials and incorporate justifiable safety thresholds. "Our recommendations are to start the selection process during development and begin to qualify components early, rather than in late phases of development, because if you have something objectionable, you can understand the potential to cause patient harm and eliminate or mitigate the risk," says Paskiet.


ADVERTISEMENT

blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
|Monthly
| Weekly

Survey
FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
Reducing drug shortages
Breakthrough designations
Protecting the supply chain
Expedited reviews of drug submissions
More stakeholder involvement
Reducing drug shortages
32%
Breakthrough designations
11%
Protecting the supply chain
37%
Expedited reviews of drug submissions
11%
More stakeholder involvement
11%
View Results
Jim Miller Outsourcing Outlook Jim Miller Health Systems Raise the Bar on Reimbursing New Drugs
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerThe Mainstreaming of Continuous Flow API Synthesis
Jill Wechsler Regulatory Watch Jill Wechsler Industry Seeks Clearer Standards for Track and Trace
Siegfried Schmitt Ask the Expert Siegfried SchmittData Integrity
Sandoz Wins Biosimilar Filing Race
NIH Translational Research Partnership Yields Promising Therapy
Clusters set to benefit from improved funding climate but IP rights are even more critical
Supplier Audit Program Marks Progress
FDA, Drug Companies Struggle with Compassionate Use Requests
Source: Pharmaceutical Technology,
Click here