The following programs are offered for the training on the certification exams conducted by the ASQ, ISPE, RAS, QAC, SCRA and PI. The training modules are prepared according to the syllbus provided by these international bodies. This course is offered both online as well as schedule training at various parts of India. CPL also provide the certificate of completion to the participants and certify the candidate as the certified professionals. this course guarantee the success in the exams conducted by these agencies. For details of the certification programs please visit the respective web pages

This is a specialized course offered for medical device auditing. this course equip the candidate for appearing the certified Biomedical auditor course conducted by the American Society for Quality(ASQ).                                                                               course details

Qualified  Pharmaceutical Professional

This course is designed for the pharmaceutical and medical device professionals who specialized in Validation, projects QA and manufacturing etc. this examination is conducted by the International society for pharmaceutical engineering (ISPE). CPL offers a comprehensive training module according to the ISPE syllabus building a confidence to attend the ISPE examination. for details of the ISPE examination visit ISPE                                                                                                            course Details

Qualified  GMP Auditor

This course provide the  advanced methodology for auditing GMP complaint facility. the corse covers all aspects of GMP auditing for Pharma, Biotech, and medical device facilities.                                                                                                     course Details

Certified Regulatory Professional

The Regulatory affair professional qualification enable the candidate to manage the regulatory requirement for drugs and devices in regulated  markets. The course is giving special emphasis on the regulatory requirement for US FDA, EU and other developed countries. The module also covers the requirement for regulation of drugs and devices in india                                                                                                          course Details

Qualified  Validation Manager

The program covers all the aspects of the validation of facilities, process and equipment in manufacturing and testing facilities.                                                               course Details

Qualified  Pharmaceutical Quality Assurance Professional

Qualified Clinical Research Associate

Qualified  Clinical Research Coordinator

Qualified  Clinical Trial investigator

Qualified  Physician Investigator