- GMP and Compliance
- Pharmaceutical Product Development
- Development and Manufacture of Effervescent Tablets
- HPLC Analytical Method Development and Validation
- Hands-on Tablet Development including the principles of pre-formulation, formulation and process dev
- Introduction to LC-MS for Pharma Industry
- Introduction to Photostability
- Introduction to Sterile Product Manufacture for New Starters and Junior Staff
- Introduction to Sterile Product Manufacture for those with a cGMP basic understanding
- Pharmaceutical Packaging - an introductory course
- Pharmacokinetics in Drug Development - an integrated approach
- Preformulation Studies for Tablet Development
- QbD and Lifecycle Management for Analytical Methods
- Quantitative Bioanalysis using LC-MS for Pharma Industry
- Stability Testing in Biological Product Development and Manufacturing
- Stability Testing in Pharmaceutical Development and Manufacture
- Tablet Formulation Development
- Tablet Formulation Development - Formulation development in practice
- Tablet Process Development, Validation and the Application of QbD
- Technology Transfer
- Pharmaceutical Manufacturing Support
- Pharmaceutical R&D Support
- In-house Training Courses
Introduction to Photostability
| Tutor : Michael Gamlen | |||
| Date | Location | Fee | |
|---|---|---|---|
| 23 November 2012 | London | £549 + Vat Book now for early bird price |  Before 28 September 2012 |
|
Book this course with Stability Testing in Pharmaceutical Development and Manufacture On the 21 - 22 November 2012 for a 10% discount |  | ||
Overview
The purpose of this course is to give an overview of photostability and where it fits in the stability testing programme and the importance of photostability. The course is highly interactive and held in a relaxed environment.
It will cover:- Why do we do photostability tests?
- Concepts and background in photostability
- Identifying drug substances most likely to absorb light and display signs of poor photostability
- Understanding photostability terminology
- Where does photostability fit in the overall stability testing programme?
- Why does photostability matter? (exercise)
Who Should Attend?
The course is designed for people working in:- Analytical Development
- Analytical Chemistry
- Stability Testing
- Technical Operations
- Research and Development Chemistry
- QA/QC
- Formulation Development
- Pharmaceutical & Biopharmaceutical Manufacturing/Production
- Product Development
- Regulatory Affairs
- GLP/GMP Compliance
Course Programme
Coffee and registration will be available from 8.30am, course proper will commence at 9.00am. We anticipate the course will finish at 5.00pm.
Formulating and manufacturing unstable products- Formulation development and evaluation for photolabile materials
- Protection during the manufacturing process
- Getting the product to the patient
- Understanding the terms and procedures used in the guideline
- Light source selection - Options 1 and 2
- Sample presentation
- Humidity and temperature control
- Selecting sample containers
- Selecting experimental conditions for stressing samples with respect to light
- Documentation - principles and practice
- Stability testing and the Quality System
- SOPs for stability testing
- Equipment validation and calibration - do the chambers work?
- Protocol development and approval
Delegate Workshop
Problems and issues for discussionAdditional Resources
Online access to comprehensive publications including all relevant guidance will be provided as well as colour copies of all presentations and case studies.
