Description:\n\nThis webinar will discuss the US’s FDA Final Rule for current Good Manufacturing Practices (CGMPs) for combination products. In particular, it is intended to better understand the cGMP requirements for enforcement purposes. \nBoth domestic and foreign manufacturers are required to establish and maintain a quality management system (QMS) to the extent applicable for combination products (e.g., drug and medical device). The speaker will discuss how firms can achieve compliance with quality system regulations as well as how to achieve compliance with drug cGMP requirements for combination products. For example, do design controls apply when a device constituent part is used in a combination product? If so, what levels of design control would apply?\nTo achieve compliance and to remain compliant with the cGMP requirements applicable for combination products, it is critical that executives and managers understand and accurately interpret the applicable requirements so that compliance to cGMP requirements can be adequately, sustainably achieved.\n\nThis webinar will provide a great opportunity to get familiar with the cGMP requirements and greatly improve your awareness and confidence.\n\nAreas To Be Covered in this Seminar:\n• Applicable Laws and Regulations\n• Definitions\n• Current Good Manufacturing Practice (cGMP) Final Rule for Combination Products\n• cGMP Requirements for A Co-Packaged Or Single entity Combination Product\n• Implementing Compliance to Quality System Regulations\n• Implementing Compliance to Drug cGMP Requirements\n• Implementing Compliance to Biological Product and HCT/P Requirements\n• Comparative Discussion on 21 CFR Parts 210/211, 600-680, 820, and 1271\n• Common Misconceptions\n• How to implement cGMPs for Combination Products\n• Best Practices: Dos and Don’ts\n• Speaker’s PASS-IT Recommendations\n\nWho will benefit:\n• CEOs\n• VPs\n• Compliance Officers\n• Attorneys\n• Regulatory Affairs\n• Clinical Affairs\n• Quality Assurance \n• R&D\n• Consultants\n• Contractors/Subcontractors\n• Anyone Interested in the FDA Drug Review and Approval Processes\n\nFor More Details:https://www.grcts.com/GRC-90054\nEmail: [email protected] |Tel: 1-248-233-2049
Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author.While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server.