Released on = December 21, 2006, 12:03 pm

Press Release Author = M. M. Chowdhury , Amreteck LLC

Industry = Pharmaceuticals

Press Release Summary = Amreteck LLC, USA has introduced pharmaceuticals cGMP
training seminar at Bangladesh, India & China to be complaint with US FDA & EU
regulations and standards. Instructors from well known pharmaceutical companies in
India and USA will conduct these training in various countries. This training will
be low cost compare to ISPE and PDA training at USA. Amreteck LLC is working hard
to bring new technolgies and training to the Asia\'s door steps. The first training
is offered in Bangladesh on March 2-8, 2007 at Dhaka, Bangladesh.

Press Release Body = An invitation has been extended to the Bangladeshi
pharmaceutical companies to join the annual current Good Manufacturing Practices
(cGMP) training sessions in Dhaka, Bangladesh. This is the first of its kind
training session in Bangladesh. Mr. Chowdhury has decided to provide this training
to help Bangladeshi pharmaceutical industries to be compliant with US FDA and
produce world class quality products and capture potential US$10 Billion export
markets in the world. To comply with international standards and produce quality
medicines are the key to capture international markets. There will be two 3-days
sessions and each session will have capacity of 25 attendees. Please email us and
reserve the seats before it's sold out.

Instructor: M. M. Chowdhury, Chemical Eng, Senior Validation Eng, MBA on Health Care
Management (On going), USA

Training Held: Radisson Water Garden Hotel Dhaka, Bangladesh

Session 1: March 3-5, 2007
Session 2: March 6-8, 2007

Fee: Only BD Tk. 15,000 (US$230) per person /session

Registration Final Dateline: February 15, 2007

Capacity: 25 persons per session

*Refreshments and lunch will be provided at the training.

Training Topics

Day 1: Current Good Manufacturing Practices (cGMP) overview, US FDA and EU
prospectus on manufacturing quality medicines, and multiple case studies from the
big pharmaceutical companies in USA.

Day 2: Strategies and techniques of validation (Equipment, computer, facility,
utilities, laboratories and cleaning), providing templates and understanding for
various validation documents and SOPs.

Day 3: Facilities Auditing, Deviations, Corrective and Preventive Action (CAPA),
Total Quality Management (TQM) settings, and Implementation of Process Analytical
Technologies (PAT).

Who needs to attend?

Managing Directors, CEOs, Validation personnel, Engineers, QA, QC, Management,
Procurement, Plant Managers, Plant executives, Project Managers, Drugs Inspectors,
Drugs Authorities, Manufacturing personnel and Regulatory personnel.

Training Advantage

1) Low cost compare to the ISPE training in USA. ISPE three days training costs
BD Tk. 125,000 (US$1900) per person in USA.
2) Enhance job performance
3) Help to produce quality medicines
4) Getting recognition of international quality training
5) Provide understanding to capture export markets with producing quality medicines
6) Provide understanding of pharmaceuticals regulations, requirements, and
standards
7) A certificate will be provided after completion of the training

Contact info:

M. M. Chowdhury, Chemical Eng (USA), MBA (On going)
CEO & Founder, Amreteck LLC, USA
\"A Leading Global Pharmaceuticals Service and Investment Advisor Company\"
Emails: MChowdhury@amreteckpharma.com
Chow7402@aol.com

Global Head Office:
637 Park Creek Court,
Gainesville, GA 30504
USA
Phone: (678) 858-5952
Email: Info@amreteckpharma.com
www.amreteckpharma.com

Bangladesh Office:
House # 110, Road # 17, Sector # 14, (3rd floor)
Uttara Model Town, Dhaka-1230
Bangladesh
Email: Farid@amreteckpharma.com


Web Site = http://www.amreteckpharma.com

Contact Details = M. M. Chowdhury, Chemical Eng, MBA on Health Care Management
Gainesville, GA 30504, USA
Ph: 678-858-5952