Active Pharmaceuticals Ingredients apollo api ,Indian Manufacturer,Indian API Exporter,Indian,Supplier,Pharmaceutical API,ACTIVE PHARMACEUTICAL INGREDIENTS in India, API Manufacturing India, API Exporter India, Domestic API Manufacturer, Pharmaceuticals Exporter India, API Manufacturer India, Indian API Manufacturer, Indian API Manufacturer, Indian API Manufacturing, Chloroquine Phosphate API Manufacturer India, Digoxin API Manufacturer India, Ergometrine API Manufacturing India, Gentamicin API Manufacturing India, Hydroxocobalmin API Manufacturing India, Isoprenaline API Manufacturing India, Pharmaceutical Formulations Manufacturer India, Contract Manufacturing Pharmaceuticals API, Pharmaceutical API Formulations Manufacturer, apollo api Pharmaceuticals Limited
Apollo Phaarmaceuticals API Manufacturers India Pvt.Ltd. .Committed to Quality excellence, complying with the National, and International Quality Standards. Customer satisfaction surpassing standards in respect of quality, reliability and services by employing quality driven staff, ensuring stringent performance standards. Concern and respect for Quality of people with continuous updating of knowledge. Our facilities compliance to Environmental and Safety Standards and Regulations.

Apollo Phaarmaceuticals API Manufacturers India Pvt.Ltd. Industries is committed towards Excellence in Quality

        Analytical development supported with Modern Instruments

         Preparation of Drug Master File

         Stability studiesDMF filings for the US.

         Analytical Method Validation


Quality System:
          is to co-ordinate the development and maintenance of the Company’s quality procedures and systems. This is achieved through vendor development, sampling and testing procedure, validation exercises, environmental monitoring and periodic audit of materials, facilities, systems and procedures, which can influence the quality of company’s products throughout the shelf-life.
 

The purity:
            That the product is free from any cross contamination or impurities which may affect on the efficacy of the product, unless those (impurities) which are determined in the pharmacopoeia and with the allowed limits. The safety :That the product always stays within the safety limits when it used by the patient.


The major duties of QA-department are as the following:
 Inspectionand monitoring in all production departments, 
2  Inspection and monitoring in the laboratories,
3  Inspection and monitoring in the warehouses,
4  Inspection and monitoring in the public utilities, in addition
5  Evaluation the suppliers,
6  Handling customers complaints,
7  Performing self inspection processes,
8  Training and qualifying the employees and the technical staff, and
9   Recall products from the market.