Two day Workshop on Introduction to GLP and GDP, Saturday 29th & Sunday 30h November 2008, New Delhi

Cliniminds, announced today one more workshop on Introduction to GLP and GDP to be held on 29th -30th November 2008 after getting huge response from previous workshops.

Delhi, India, November 06, 2008 --( A Laboratory Perspective for Regulatory Studies in New Drug Development
Saturday 29th & Sunday 30h November 2008, New Delhi.

Cliniminds –Academy for Clinical Research Training & Management and Therapuces now join hands to bring this program to India.

Therapuces LLC has developed highly-targeted training Therapuqest with a focus on regulatory process Good Lab Practice (GLP) for the drug /therapeutic and its service industries.This service is offered to develop the resources to match the Global standards. This training focuses on regulatory details that are necessary for the industry to follow in the approval of Drugs/therapeutics around the world.

This course provides participants with an understanding of basics of the GLP terminology and acceptable practices in testing and compliance. The course covers current regulations ,as well as ,current issue involving implementations. Attendees will get a clear understanding of the needs for thorough documentation and also wholesome education on the regulatory processes. Also includes a discussion of functions related to Quality Assurance responsibilities and the need to effectively audit for GLP compliances. Successful audits are often a result of good planning and interaction between QA staff and management.

Who Should Attend?

Scientists / Managers-Scientific / Regulatory Affairs and Compliance personnel / Technicians / Pharmaceutical professionals / Quality Assurance Managers / Auditors / Production Managers / Executives interested in implementing GLP.

Following Sessions will be covered during the workshop by industry experts:

- Responsibilities and requirements of GLP -Laboratory set-up and guidelines
- Records Management -Good Documentation Practice
- GLP Special requirements -Analysis of samples
- Electronic Records -Data storage and retrieval
- Operation of the Archive -Reporting of data and documents
- Inspections -Investigations and outcomes
- Moving from compliance to business improvement

Course Objectives: Upon completion of the workshop, the attendee should be able to understand, what is the basics of GLP, How to set up a Laboratory space for Regulated work, Training requirements for the Lab personnel, differentiation of GLP requirements from GMP requirements, Why and How to Document the details of a regulated study

Dates of Workshop: 29th-30hth November 2008 (Saturday & Sunday)

Timings: 9 a.m. to 5 p.m.

Last Date of Registration: 25th November 2008.

Number of Seats: 15

Registration Fee: Rs.10000/- per person. Rs.8000 per person for 3 or more participants from one organization. Spot registration can also be done (subject to availability of seats)

Payment Mode: By Cash or Bank Draft/Cheque favoring 'Tenet Health Edutech Pvt. Ltd., payable at New Delhi. You can also make payment by Credit Card through their website –

Workshop Venue: Cliniminds, C-55 First Floor, Preet Vihar, Main Vikas Marg, Delhi 110092

Certificates: Certificates of Participation will be issued to all participants.

For Registration & Information Please Contact

C-55 First Floor, Preet Vihar,
Main Vikas Marg, Delhi 110092; Mobile: 9871072560; 9873888671; 9810068241

Email:; Website:

Cliniminds-Academy for Clinical Research training and Management
Jitto Thomas