BioPharm International - March 2022

BioPharm International March 2022

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12 BioPharm International Quality and Regulatory Sourcebook eBook March 2022 www.biopharminternational.com Remote Inspections— Lessons Learned This article discusses select industry experience with regulatory authorities utilizing alternative mechanisms for assessing compliance as part of their review and approval of existing marketing authorizations or new applications. I n February 2020, travel ceased as the COVID-19 pan- demic began to emerge. Since that time, we have come a long way with stay-at-home orders, social distancing, testing, tracing, and quarantine. Countries that imple- mented aggressive public health measures have had fewer cases and fewer deaths. The regulatory authorities also ceased to travel and were forced to utilize alternative mechanisms to assess industry compliance and review and approve new applications. This article discusses select industry experience with regulatory authorities utilizing alternative mechanisms for assessing compliance as part of their review and approval of existing marketing authorizations or new applications. Until the time of the pandemic, the norm was that inspec- tions would be performed as in-person on-site inspections. In the case of the European Union, Amended Directive 2001/83/EC, article 46(f) (1) explicitly states, "the holder of the manufacturing authorisation shall verify compliance by the manufacturer and distributors of active substances with good manufacturing practice and good distribution practices by conducting audits at the manufacturing and distribution sites…" [emphasis added by author]. Alternative inspection forms (i.e., remote inspections) weren't foreseen. As there is no globally accepted def i- nition of such an inspection form, the authors will refer to what is provided in the Parenteral Drug Association's (PDA's) Points to Consider in Remote and Hybrid GMP/GDP Inspections document (2): JAMES STUMPFF, RPH, is Principal Consultant at Parexel International. SIEGFRIED SCHMITT, PHD, is Vice President Technical at Parexel International. JAMES STUMPFF AND SIEGFRIED SCHMITT Quality and Regulatory Sourcebook Regulations: Inspections Kadmy - Stock.adobe.com

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