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Thursday, December 14


GMPS DYNAMICS: UNVEILING DEVELOPMENTAL PHASES

GMPS Dynamics: Unveiling Developmental Phases

By Comply Rules
229 followers
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DATE AND TIME

December 14 · 4pm - December 15 · 8pm CET


LOCATION

Online


REFUND POLICY

Contact the organizer to request a refund.
Eventbrite's fee is nonrefundable.


ABOUT THIS EVENT

 * 1 day 4 hours
 * Mobile eTicket

Date: Dec 14-15, 2023

Time: 10 AM - 2 PM EST

Duration: 8 Hrs., 4Hrs/Day

Group Packages: Please contact Sam@complyrules.com

Early clinical trials are conducted to establish the initial safety of a drug.
The studies are generally in a small number of healthy subjects and use lower or
ranging doses of the drug product. Therefore, only small amounts of
investigational material are required. In-order to not undertake substantial
costs and to reduce regulatory burden during these early stages, the FDA has
established guidelines to allow early-stage investigational products to be
manufactured under “phase 1 GMPs,” allowing flexibility in some of the rigorous,
expensive, and time-consuming requirements. As clinical development progresses,
evolving into “phase 2 GMPs” and into commercialization with a methodical and
comprehensive planned approach can save substantial time and expense.

This master program will include a detailed review of the current regulations as
must be followed for commercialization as well as guidance documents with the
flexibility in the interpretation of the regulations for earlier stages of
manufacturing in compliance with GMPs to support early clinical trials.

Regulatory strategies, logistical considerations, and GMP-staging plans, options
and alternatives, including raw material selection and receipt, vendor selection
and management, stability programs, packaging and labelling, SOPs, documentation
requirements, and validation will be discussed and explored through
interpretations and case study examples.

Program Objective:

Employ strategies within your company to save time and money in advancing
clinical development.

This master program will provide the information and tools that you need to
understand different baseline GMP requirements for each stage of development;
beginning with needs for IND submission and phase 1 studies, progressing to
phase 2, phase 3, NDA/BLA submission, and commercialization.

Options to explore and considerations for each will be discussed so that you
have tools to develop and implement strategies for your organization using a
phase-specific staging program of GMP requirements.

Chapter 1- Overall drug development and GMP timing

 * Planning for the IND
 * Gaining feedback on GMP plans
 * Resource and product consideration in planning
 * Quality Unit and oversight
 * General GMP considerations for every stage/phase

Chapter 2- GMP regulations and interpretation for early stages Part 1

 * Facility
 * Personnel
 * Equipment
 * SOPs
 * Documentation

Chapter 3- GMP regulations and interpretation for early stages Part 2

 * Vendor selection, oversight, and management
 * Quality agreements and contracts
 * Auditing
 * Complaint handling
 * Change control
 * Investigations
 * SOPs internally and externally
 * Record review and batch release
 * Packaging and labeling
 * Updating the IND

Chapter 4 - Evolving processes to commercialization

 * Quality unit roles and responsibilities
 * Facility updates Change control
 * Preparing for the NDA/BLA
 * Validation plan
 * Master batch record
 * Electronic data collection
 * Packaging and labeling
 * Distribution
 * Instructions for use, storage, and handling

The following topics will be discussed to provide the foundation and basis for
advancing drugs into clinical development from research and providing required
information to the FDA regarding these products.

 * Moving a Product out of R&D
 * CMC Requirements for an IND Study and commercial
 * Good Manufacturing Practices: Basics for Beginners
 * Raw Material Management

Specifics topic will include:

 * Issues with research-grade material used for laboratory and non-clinical
   testing
 * Optimizing manufacturing processes
 * Raw material requirements and process development
 * Assessing scalability of manufacturing
 * Planning the CMC for a potential IND
 * Study Essential elements of the CMC section of an IND
 * Characterization of the active ingredient and finished product
 * Various kinds of products: drugs, biologics, botanicals, diagnostics, medical
   device
 * Manufacturing facility personnel equipment and requirements
 * Core principles of GMP regulatory requirements for all different products…
   drugs to medical devices
 * Customizing regulatory compliance to a given product
 * Role of discussions with the FDA
 * Planning for the early stage with an eye toward large scale manufacturing
 * Vendor management
 * Raw material handling issues for early-stage products
 * Manufacturing step development

The following topics will be discussed to provide the requirements for
early-stage products of different types and for vendor selection and management.

 * The scope of the FDA guidance documents
 * Acceptable practices and tips
 * GMP requirements for exploratory clinical studies
 * Specific requirements for drugs, biologics, and combination products
 * Specific issues for various kinds of combination products
 * Combination products with one or more new components
 * CMC issues for 505(b)(2) products
 * GMP and QSR: which to follow for a combination product
 * Introduction to process validation for early-stage manufacturers
 * Step by step introductions for process validation
 * Process validation reports and other documentation
 * Developing SOPs based on validation processes
 * Logistics of using contract manufacturing organizations for early-stage
   products
 * Pilot-scale manufacturing requirements GMP-grade and non-GMP grade
   manufacturing
 * Benefits and challenges with using local and international vendors


TAGS

 * Online Events
 * Things To Do Online
 * Online Classes
 * Online Science & Tech Classes
 * #gmps
 * #online_workshop
 * #online_event
 * #online_classes
 * #online_training


ABOUT THE ORGANIZER

Organized by
Comply Rules
229 followers
 * Contact
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$849 – $5,943
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