Webinar on Combination Drug/Device Products cGMPs - Final Rule

Description :

This training on combination product regulations will evaluate the chief areas of concern or change in the new cGMP requirements for combination products, 21 CFR Part 4, and clarify many of the issues and questions that arise involving combination products.

There has been much past confusion on the production and handling of drug / device (and/or biologics) combination products. Companies involved in the production of such products have pieced together what they've considered the applicable elements of the pharma and device cGMPs, 21 CFR 210/211 and 820; sometimes with ambiguous advice from the agency, resulting in some disagreements during compliance audits.

Do not let yourself or your company be caught off guard by the new cGMP requirements for combination products. Attend this training to enhance your awareness of these new cGMP requirements and modify internal audits to match this FDA shift. This training will be a step-by-step review of the key elements of the U.S. FDA's new final rule, "Current Good Manufacturing Practice Requirements for Combination Products", 21 CFR Part 4. The presenter will evaluate and clarify many of the pertinent issues and questions that arise involving combination products.

This session will provide valuable assistance to all regulated companies in evaluating their existing or proposed cGMP compliance and internal audit emphasis for the production of combination products, as a sub-contractor or primary manufacturer. Once you have recognized the danger and likely locations of potential problem areas, a company can evaluate / perform a gap analysis, and then put in place the necessary fixes to ensure compliance to the new rule.

Areas Covered in the Session :

The Four Basic Types of Combination Products

Two or more of device, drug, biologic;

Physically combined; or

Packaged together; or

Packaged separately but intended for use only with another, different type of medical product ("cross-labeling").

The CGMP "Operating System"

Constituent Parts

Applicability of 21 CFR 210/211, 600-680, 820, and 1271

The Two Ways to Compliance

Single-type Constituent Part Facilities

How to Address cGMP "Conflict"

Who Will Benefit:

This training applies to personnel / companies primarily in the pharmaceutical, medical device, and biologics fields. The employees who will benefit include:

Senior management

Regulatory affairs

Quality assurance

Production

Engineering

All personnel involved in a U.S. FDA-regulated environment; especially those involved in cGMP compliance of affected regulated combination medical products

For more information and enquiries contact us at

Compliance Trainings

5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada 
Customer Support : #416-915-4458 
Email : support@compliancetrainings.com

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