Quality
Accountable for Every Pack
Our ISO 9001:2015 quality management system covers the marketing and sales of pharmaceutical products, cosmetics, medicines, medical devices and dietary supplements. That is the exact scope on the certificate, and we do not describe it as anything wider.
We do not manufacture. What we control is which units make our products, what is checked before a batch is accepted, and what paperwork follows it to the distributor. Those three things decide whether a partner can stand behind the stock in their godown, so that is where our system puts its effort.
- A manufacturing unit is qualified on its licences, GMP status and audit history before any batch is placed with it.
- Every consignment is traceable to its batch, its unit and its certificate of analysis.
- Prescription medicines move only through licensed channels, under our own wholesale drug licence.
- Nothing is claimed on this website that we cannot produce a document for.
Certified, Licensed and Audited
Every claim on this page is backed by a document you can open and read for yourself. Certificates are published in full, exactly as issued.
ISO 9001:2015
Marketing and sales of pharmaceutical products, cosmetics, medicines, medical devices and dietary supplements
GST Registration
Regular registration, effective 13 April 2022
Certificate of Incorporation
Incorporated 1 March 2021 under the Companies Act 2013
Six Checks Before a Batch Reaches You
Manufacturing happens at our partner units, so these are the controls we hold them to. Each one leaves a record we can produce later.
Unit Qualification
Manufacturing licence, WHO-GMP status and audit history are verified before a partner unit is approved. Approval is reviewed, not granted once and forgotten.
Raw Material Control
Active ingredients and excipients are sourced to pharmacopoeial grade, against the supplier certificate of analysis held at the manufacturing unit.
In-Process Checks
Weight, hardness, fill volume and related parameters are monitored during manufacture, to the specification agreed for that product.
Finished Goods Testing
Assay, description, dissolution and, for sterile products, sterility and pyrogen testing, are completed before a batch is released.
Batch Release
No consignment is dispatched without its batch record and certificate of analysis on file. That document is what makes a complaint traceable.
Storage and Transit
Products are stored and shipped to the conditions printed on the label, with temperature sensitive lines handled separately from ambient stock.
What You Can Ask For, and What Binds Us
Every document below is available to a partner on request, no reason needed. The statutes beside them govern how we supply and how we advertise.
Available on Request
- Batch-wise certificate of analysis for any consignment supplied
- Copy of our wholesale drug licence, Form 20B and 21B
- ISO 9001:2015 certificate with its current validity
- GST registration certificate and company incorporation details
- Product literature with full composition and pack details
Write to info@axventiclifesciences.com with your firm name and the batch or product concerned.
We Operate Under
- Drugs and Cosmetics Act 1940 and the Drugs and Cosmetics Rules 1945
- Drugs and Magic Remedies (Objectionable Advertisements) Act 1954
- Legal Metrology (Packaged Commodities) Rules 2011, for pack declarations
- Digital Personal Data Protection Act 2023, for enquiries made through this site
This is why the site carries no treatment claims, no prices and no direct sale of medicines to the public.
How We Handle a Complaint
Certificates are easy to publish. What matters to a distributor is what happens the day a batch does not look right, so here is that process.
Report It
Write to info@axventiclifesciences.com with the product name, batch number, expiry and what you observed. A photograph of the pack and the strip helps.
We Acknowledge
You get a written acknowledgement within one working day, with a reference you can quote in any follow up.
We Trace the Batch
The batch record and certificate of analysis are pulled, and the complaint is raised with the manufacturing unit that produced it.
You Get It in Writing
The finding comes back to you in writing, together with what is being done about the remaining stock of that batch.
Need a Document for a Specific Batch?
Send us the product name and batch number and we will share the certificate of analysis along with any licence copy you need.