The plant of Navana Pharmaceuticals Ltd. (NPL) is situated at the near of Capital city Dhaka. The plant aims to be as the most modern and one of the largest formulation units in Bangladesh. This plant in terms of Quality standards is at par with the best in the Domestic companies.

The fully integrated manufacturing facility offers a broad basket of blockbuster products, strong product development capabilities and all encompassing emphasis on total quality management.

The design concept for the facility incorporates the latest technology in terms of layout, flow of men and material. HVAC systems and the treatment of water. Care is taken to see that the facility complies with all International Regulatory guidelines and cGMP: This manufacturing facility is capable of producing oral solids such as tablets, capsules, dry powder for oral suspension, oral liquids such as suspensions and syrups.

Quality Assurance:

At NPL all actions are driven by a single-minded commitment to quality. The principles of Total Quality Management pervades all departments and are a way of life for the workforce.

The fully equipped, sophisticated Quality Control laboratories. Installed with latest computerized analytical instrumentation and equipments, control and test every stage of formulation development and production, from raw materials to packing materials to finished products besides in process testing. Special emphasis is laid on Validation and Stability Studies.

Complementing all the latest instruments and equipments is a dedicated team of highly qualified and experienced scientists. Continuous training and up-gradation programs ensure that employees are kept abreast with the trends and demands of a dynamic Regulatory environment.

Regulatory & Documentation:

Today’s fiercely competitive and highly regulated markets demand rigorous design and management of product development and registration strategies for success.

Critical time is saved in getting the product to the market in optimum period for submission to the Regulatory authorities. At NPL a team of highly Qualified Pharmacist, Biochemist and Microbiologist are engaged and technical professionals are working as part of Regulatory Affairs. Quality Assurance and Documentation Department provide services including:
· Domestic and International registrations
· Technical package containing Pharmaceutical and Therapeutic updates.
· Site Master File, Abbreviated Applications andDossiers.
· Liaison with Regulatory authorities for Audits, Inspection and Technical Queries.