- 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 Sterile Product Manufacture for New Starters and Junior Staff
No Course Dates Currently Available
Overview
To provide training to personnel who are new to the Pharmaceutical or Biotech Industries and have no understanding of cGMP and who intend to work with sterile products, development, manufacturing, registration and facilities.
The course will include:
A comprehensive background in sterile product manufacturing, regulations and facilities.
Adherence to cGMP and the consequences for non-compliance. How to initiate development of new formulations, manufacturing, environmental and product monitoring. Modes of
sterilization and types of products.
Who Should Attend?
The course is ideal for new starters or junior staff working in the Pharmaceutical or Biotech industries who will be exposed to a sterile manufacturing facility or who will be involved in the development of new products. This is an introductory course and the level of detail will be as a broad based overview.
- Clinical Trials Manufacturing Scientists
- Development Scientists
- Regulatory Affairs Personal
- Pharmaceutical Production Personnel
- Quality Control and Quality Assurance Personnel
Course Programme
Day One (9am - 5pm)
Background:
- What is a sterile product? Classification of products. Why are they sterile?
- Basic microbiology. The Regulatory environment.
- cGMP
- Facilities and processing. The impact of personnel and materials
- Environmental Monitoring. What is the difference and the impact or viable and non-viable contaminants.
Day Two (9am - 5pm)
- Dosage Forms: syringes, ampoules, vials and others
- Sterilisation: Overview of methods of sterilisation, autoclave, dry heat oven, radiation, filtration and EtOH exposure.
- Aseptic vs. Terminally sterilized, How do you decide?.
- Areas of specialization. Where do I go from here?
