Auditing an Active Pharmaceutical Ingredient (API) Contract Manufacturing Organization (CMO) - Webinar By GlobalCompliancePanel

Website https://www.globalcompliancepanel.com/control/w_product/~product_id=600464?channel=mailer&camp=webin | Edit Freely

Category Health Care, Medical Device, Compliance Training

Deadline: May 18, 2011 | Date: May 18, 2011

Venue/Country: Wilmington, U.S.A

Updated: 2011-04-12 21:58:39 (GMT+9)

Call For Papers - CFP

API manufacturing has similar regulatory GMP expectations as drug products, but not identical in is specific requirements and application. The nature of API manufacturing and its usual purification processes all influence how an API process should operate. Knowing what the FDA expects and how these regulators apply API GMP is important to API purchasers and drug product firms. Reducing risk and protecting the quality of a Drug Product (DP) is critical to the DP firm's success. The webinar will focus on the Q7 and FDA GMP requirements, what are the key contractual requirements and what should be negotiated and documented within quality agreements with a CMO firm.

Why Should You Attend: Attending this webinar will help you identify what you need to know and examine during an audit of your CMO or API suppliers. The webinar leader will help you identify key regulatory and industrial issues associated with API manufacturing. You are purchasing more than a chemical or biological material. You are purchasing a material that can carry with it hidden risks if not properly examined and controlled. Such examination is not always productive if you rely simply on testing protocols. You need to learn where to look and what to focus on during any on-site audit. While understanding the applicable GMP is important, how to apply the GMP and what to establish with a CMO is critical to your supply chain.

Areas Covered in the Session:

* Examine key elements of an API audit

* Audit preparation

* The audit itself

o Opening Session

o Audit itself

o What to look for?

o Discussion of findings

o Suggestions and experience

* Closing Meeting

* Who should participate in audit

* Who should attend openning and closing sessions

* Audit Reports

* Follow-up Actions

* Agreed upon Schedules

* Follow-up Audits

Who Will Benefit:

* Supervisors and Managers in Manufacturing

* Supervisors and Managers in Quality

* Engineering

* Maintenance Supervisors and Managers

* Warehousing and Materials Management Supervisors and Managers

Price List:

Live : $245.00

Corporate live : $995.00

Recorded : $295.00