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Welcome To The Aan Pharma Pvt Ltd

Aan Pharma pvt. Ltd. (APPL) is established in 1994 by the highly experienced promoters in our field of pharmaceuticals. They are in this respective field since last two and half decades. The main goal of the company is to provide low cost prescription medication....

RESPONSIBILITIES

Being the overall in-charge of the plant , takes care of every affairs and ongoing responsibilities. He is in-charge of overall activities of plant from concept stage to completion.

HANDLING OF MATERIALS

Quality Assurance Department finalizes detailed specification, methods of analysis, testing methods and also prepares a list of approved vendors after vendor rating and vendor evaluation.

QUALITY ASSURANCE

It is the sum total of the organized arrangements made with an object to ensure that the products will be of quality required for their intended use.

QUALITY POLICY

Mission’s Quality Policy has a broad base, with stringent specifications to ensure all Quality parameters.

TESTING

While adequate facilities are provided in-house for all testing and evaluation, for some of the tests where it is not commercially viable as yet, outside assistance is obtained.

STANDARD OPERATING PROCEDURES

Documented SOPs are available for each activity. They are prepared by the Department in-charge, approved by the QA Manager and authorized by the President.

Product Visual

Brief Overview

Aan Pharma Pvt. Ltd. (APPL) is promoted by the highly experienced promoters in the field of Drug and Formulations production. They are in the line of Pharmaceutical production since last so many years. Basically they are based at Ahmedabad which is considered to be a pharmaceutical hub of the country as so many giant pharmaceuticals companies of India are situated in and around Ahmedabad.

APPL is engaged in the manufacturing of Pharma formulations in respective sections of Tablets, Capsules, Liquid orals and Ointments.

C.M.D.
Mr. Ashvin Shah, Aan Pharma Pvt. Ltd.

DOCUMENTATION

Every product has an approved MFR which gives details like Brand Name, Generic Name, Mfg. Lic. No, Shelf life, Storage Conditions and Packing Style and Quantity of RM / PM for a standard Batch Size, Process Details, Precautions, In-process Checks, Reconciliation at various stages of Production, Yield, Packing Details etc.
BMR formats are computer generated. They are essentially copies of MFRs giving detailed process steps. Completed BMRs are retained securely for a period of 5 years or one year after the expiry of the product whichever is later by the QA Department.
Documented SOPs are available for each activity. They are prepared by the Department in-charge, approved by the QA Manager and authorized by the President.
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