 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
Compliance Courses
» Compliance Seminars®
International courses with world leading compliance specialists
- Auditing & Inspections
- Biopharmaceuticals & Biotechnology
- Clinical Trial Materials
- Compliance Validation
- General GMP
- Laboratory Operation
- Medical Device
- Sterile Pharmaceuticals
Courses in local languages
In-House and open courses for all levels in
the following languages:
» FRANÇAIS (FR/BE/CH)
» SVENSKA
» ITALIANO
» On-line courses in statistics
Basic statistics for QC- lab and R&D personnel
International courses with world leading compliance specialists
- Auditing & Inspections
- Biopharmaceuticals & Biotechnology
- Clinical Trial Materials
- Compliance Validation
- General GMP
- Laboratory Operation
- Medical Device
- Sterile Pharmaceuticals
Courses in local languages
In-House and open courses for all levels in
the following languages:
» FRANÇAIS (FR/BE/CH)
» SVENSKA » ITALIANO» On-line courses in statistics
Basic statistics for QC- lab and R&D personnel
- Batch Record Review and Investigations
- CGMP: Interpretation and Application
- Compliance for Biopharmaceutical API Process Validation
- Compliance to Clinical Safety and Pharmacovigilance Regulations
- Validation and Qualification Compliance Requirements
- Practical Approaches to Global GMP for Investigational Medicinal
Products (Clinical Trial Materials) - Quality System Requirements & Industry Practice
 |
» Recommendations on how to apply Copenhagen May 4 2009 |
Lundén/Ellow ab and EuroGMP AB • Tjädervägen 10 • SE-181 56 Lidingö • SWEDEN • Phone: +46-(0)8-544 811 60 • e-mail: info@key2compliance.com