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Trainings Application Form
Information about the Applicant
Name, Surname:
Email:
Telephone number:
Mobile Phone number:
Postal Address:
Occupation
Information about the organization:
Name of the organization:
Address of the organization:
Telephone number of the organization:
Fax number of organization:
E-mail of the organization:
Website address of the organization :
General Information
Requested training/consultancy service(s):
Analytic Method Validation (in compliance with EMA, FDA and ICH Rules)
Calibration and Modern Calibration Management
Cleaning Validation
Corrective and Preventive Actions Training (CAPA)
GC/MS– Gas Chromatography & Mass Spectrometry and Practical Method Development Training
GMP – Good Manufacturing Practices Update Training
GMP documentation
HPLC-Practical Method Development Training
Impurity and Degratation Training
ISO 13485 – Quality Management Systems for Medical Devices
ISO 17020 – General Terms for Operating Different Type Examination Entities
ISO 17025 – General Terms for Experimental and Calibration Laboratories Qualification
ISO 9001:2000, ISO 9001:2008
MDD 93/42/EEC – Medical Devices Directive
Out- of- Specification (OOS)
Process Validation Training – Risk Based Approach
Process Validation, Quality By Design, Design Of Experiments
Product Quality Review (PQR)
Product Quality Review (PQR)
Qualification Training – Risk based Approach
Risk Management and Risk Analysis Techniques Practical Training (FMEA, FTA, ISHIKAWA, Filtration techniques)
Site Master File (SMF)
Stability Testing & Photo Stability Testing
Training on Change Control (CC)
Training on Computerized System Validation (Risk Based)
Training on Standard Operating Procedures (SOP)
Training on Validation Master Plan - VMP
User Requirements Specification (URS)
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Number of Attendants:
Requested date for the trainings/consultancies:
Your expectations of the training/consultancy:
Other information you would like to add:
