Expert guidance through today’s regulatory landscape
InterProQRA is a dynamic, global consulting practice specializing in CGMP compliance and FDA regulatory adherence. We deliver comprehensive solutions to pharmaceutical/biologic companies of every size.
Our team is uniquely qualified to help you manage compliance and regulatory challenges and to efficiently address those that may arise. Combining decades of boots-on-the-ground FDA evaluation and enforcement experience with extensive consulting work for pharmaceutical clients, our team applies the insight and foresight that only comes from working both sides of the Quality table.
CGMP Compliance Solutions
- Regulatory preparedness/gap analysis
- Auditing; qualification, pre-inspection and due-diligence
- 483 Response
- Warning Letter
- Consent Decree
- Annual CGMP
- Aseptic processing
- How to interact with the FDA
- Design guidance
- Audits during construction through validation
Need Regulatory Guidance? Get Help From The Source
Click below to download our brochure and learn more about how you can anticipate and resolve violations before they happen.