Our State of the art manufacturing plant is housed in a double story building encompassing an area of 23,000 sq feet. Manufacturing undergoes continuous improvement in production and quality assurance facilities to ensure the quality of products as per international standards.
The plant is segregated into two units for manufacturing sterile products (Injections, Ophthalmic Drops, Ointments) and non Sterile products (Tablets, Capsules, Dry Powder, Topical Ointments, Creams, Lotions and Liquids).
Qualified and experienced staff supervise the manufacturing process in accordance with GMP and WHO guidelines.
On line and periodic inspections are carried out during the manufacturing process to ensure compliance with quality standards. The production department is sub divided into the following departments:

. Manufacturing
. Packaging
. Warehouse for Raw, Packing material and finished goods.
. In process quality control
. Finished product quality control and microbiological testing facilities.


Quality Assurance:

The management at ATCO is fully conscious about quality assurance and always views this as a top priority. Right from the acquiring of incoming materials, to the release of finished products, QA plays an essential role. The environment is controlled in all the critical manufacturing areas, where factors like dust and humidity, that may affect quality, are eliminated.
Parenteral and other sterile products have special air handling and A/C systems, that comply with GMP and WHO requirements.
The Quality control laboratory is situated in the same building and is sufficiently equipped and organized. Qualified and experienced staff run this department and the head of QA reports directly to the Managing Director. This independent department performs the following essential functions:

. Setting standards and procedures.
. QC testing of incoming materials, bulk, semi-finished
  and finished products.
. Developing products' stability protocols.
. Training of staff periodically.
. Surveillance of marketed product.
. Regulatory affairs.
. Post production documentation.

The QC department also pays special attention to regular microbiological tests of the products and the environment by taking samples from the atmosphere of the factory area.