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Elixir Pharma

Elixir Pharma is on a mission to offer products & services to Global Life Science companies in such a manner that our customers are able to bring innovative, affordable and quality products to their customers in the fastest and in the most economic manner and by doing so, Elixir Pharma will have-

Delighted stakeholders
Improved quality of life of people around us
Maximized return on investments
Reduced health care burden on General Public and Governments worldwide

To accomplish this objective, we commissioned our first site in the month of July 2010 within estimated timelines at Naroda, GIDC in Ahmedabad and have plans to add a second site in a years’ time.
At this site, we have a highly motivated team of scientists & engineers; a PRD lab, a Kilo Lab, a cGMP pilot plant, commercial manufacturing plant, QC/QA and are suitably placed to quickly develop & supply quality products and partner with you in solving challenging development, scale-up & regulatory requirements of your development programs across the development cycle.

Company Album

Factsheet

Basic Information

Nature of Business	Manufacturer
Additional Business	Retail Business Factory / Manufacturing Office / Sale Office Wholesale Business Export Import Supplier of Services
Company CEO	Dinesh Patel
Total Number of Employees	26 to 50 People
GST Registration Date	01-07-2017
Legal Status of Firm	Partnership
Annual Turnover	25 - 100 Cr
GST Partner Name	Beenaben Bipinchandra Patel Zalak Harsh Patel

Statutory Profile

Import Export Code (IEC)	0805012648
GST No.	24AACFE0122B1ZJ

Testing Facilities

Stringent quality control for all stages of manufacture and delivery.
Quality control laboratories are well equipped with the latest instrumentation.
Quality up-gradation of our products is a regular developmental feature.
Well Equipped Micro Biology Lab.

Quality Policy / Processes

Preparation & approval of various validation protocols like process validation protocol, rework & milling validation protocols.
Preparation & approval of stability protocols, cleaning records & batch records.
Preparation of validation reports, stability reports of starting materials & actives.
Preparation of various SOPs related to production, testing, release, packaging & labeling of the APIs.
Preparation & approval of various IQ & OQ protocols.
Execution of IQ/OQ & PQ in co-ordination with the technology department and equipment supplier & preparing IQ/OQ reports.

Aim / Vision / Mission

Vision
To establish ourselves as a reliable, cost competitive, quality products and chemistry service provider to Global Life Science Companies and achieve annual sales of USD 30 million by 2015
To identify growth areas, expand infrastructure, products & services portfolio and be an integrated solution provider to Global Life Science Companies with annual sales of USD 100 million by 2020
To acquire and maintain leadership position in chosen products & services areas Globally
To be a recognized partner of choice to Global Life Science companies by effective client servicing & technological excellence.
We are here to offer products & services to Global Life Science companies in such a manner that our customers are able to bring innovative , affordable and quality products to their customers in the fastest and in the most economic manner, by doing so, we’ll have-
-Delighted stakeholders.

Mission :

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