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New study will reveal bio/pharma practices and performance on quality issues.
With infrequent inspections by regulatory authorities--and time lapses between the identification of a violation and remedial or regulatory action--patients place trust in the self-enforcement of quality practices by API and drug manufacturers. How is the bio/pharma industry addressing quality practices?
Based on FDA data, the number of warnings for API and drug product manufacturing nearly doubled from 2015 to 2016 (1). Typical warning letter violations included failure to validate processes, determine a root cause, implement corrective action and preventive action (CAPA) plans, establish or follow written procedures for the prevention of microbiological contamination, conduct routing environmental monitoring tests, and investigate unexplained discrepancies in batches. The agency also cited firms for the lack of quality plans, supporting data, control over data and laboratory records, and scientific evidence to support procedures.
In fiscal year 2016, FDA issued almost 700 Form 483 observations, slightly above the average issued in the previous three years (2). The most frequently cited observations were:
What happens when FDA is not watching? In an industry-wide study, the editors of Pharmaceutical Technology examined quality practices as described by experts in quality, regulatory affairs, analytics, and manufacturing and production roles at companies serving the US market. The results will be revealed in a session, Quality Practices: Meeting and Exceeding Regulatory Expectations, at the CPhI North America event (May 16-18, 2017) in Philadelphia.
The survey examined the role of the quality control department in a bio/pharma organization and its impact on GMPs, the prevalence of quality management systems and quality-by-design programs, factors contributing to quality problems, and the company’s approach to regulatory compliance.
Survey respondents also evaluated the performance and contributions of FDA in providing information to address quality-related problems; the usefulness of FDA regulations, guidance documents, and agency expertise; and initiatives such as quality metrics and data integrity. Respondents also commented on actions FDA can take to improve the quality of drugs manufactured for the US market.
The study participants also commented on equipment failures, production errors, inadequate method development, and failures by the quality control team. Relationships with contract service organizations and materials and equipment suppliers--including quality agreements and supplier oversight--are also reviewed.
The presentation is scheduled for May 17 from 2:30-3:15 pm in the exhibit hall. For more information, visit www.cphinorthamerica.com.
1. FDA, Inspections, Compliance, Enforcement, and Criminal Investigations, accessed Dec. 20, 2016.
2. FDA, Inspection Observations, accessed April 20, 2017.
Vol. 41, No. 5
When referring to this article, please cite it as R. Peters, “Keeping an Eye on Quality," Pharmaceutical Technology 41 (5) 2017.