21 CFR, Parts 210 and 211

Troy Fugate is the VP and Co-founder of Compliance Insight (www.compliance-insight.com)
Compliance Insight is a leading FDA regulatory and quality assurance consulting firm that offers a range of services to assist companies in navigating the complexities of FDA regulations. With their in-depth knowledge and expertise, Compliance Insight provides invaluable guidance and support to ensure compliance with FDA requirements.
One of their key services is assisting companies with the 510(k) process. They understand the intricacies involved in preparing and submitting 510(k) applications for medical devices. Compliance Insight helps clients gather the necessary data, conduct thorough reviews, and ensure the application meets all regulatory standards, streamlining the path to FDA clearance.
In addition, Compliance Insight has extensive experience in the emerging field of cell and gene therapies. They offer specialized guidance on navigating the unique regulatory landscape for these innovative therapies, helping clients understand and meet FDA requirements to bring their life-changing treatments to market.
Another area of expertise for Compliance Insight is providing assistance with 483 and Warning Letter response and remediation. In the event of an FDA inspection resulting in observations or deficiencies (captured in Form 483), Compliance Insight supports companies in developing comprehensive and effective responses. Their team works closely with clients to address each observation, develop appropriate corrective actions, and ensure timely and compliant resolution.
Whether it's navigating the 510(k) process, advancing cell and gene therapies, addressing 483 observations, or more; Compliance Insight's services encompass comprehensive regulatory support to help companies achieve and maintain FDA compliance, fostering successful product development and market approval.
For more, visit us at www.compliance-insight.com

[@gustavopoueymirou-ortiz7981]

Excellent training. You got a 10 +

[@benseghirloundja7274]

Great training thanks a lot.

[@joja2568]

Thank you. Very helpful!

[@nareshtyagi2009]

Very good thank u.

[@pharmamanu7]

Lecture is clear and very useful,, Thank you Sir

[@curleyps6122]

thank you for the training
though i have few questions
may i know the exact difference between Batch and LOT
what is in-process control
would you suggest me how to obtain and remember all the 21cfr parts for GMP knowledge
thank you

[@thehealer8330]

What is the use ICH guidelines when 21 CFR already present? Sir plz give ur response. And how it corelate with each other?

[@sakshigupta4177]

Very informative sir 🙏..... thanks

[@JayhawkGuitar]

Thanks for this overview. Very helpful.

[@sakshigupta4177]

Have you made a video on EC Principles of GMP (Directive 91/356/EEC) Article 6 to Article 14
If not then please share your knowledge on the above topic 🙏..... waiting for your next session

[@sumagatla9446]

I also want this topic sir