Marketing

Parth Antibiotics has a dynamic and capable Management, Sales and Project team with proven experience in handling various projects due to which have exclusive agency from more than 200+ manufacturers and work over 600+ products like Cephalosporin’s, Beta Lactam, Steroids, Hormones, Macrolides, Quinolones, Anti-Hypertension, Carbapenems Anti-Diabetic, Cardiovascular and many more.


With a strong marketing team, we have succeeded in catering clients from Abbott Ltd to Zydus Cadila. We have more than 1500+ cliental base from across 25 countries with a projected group turnover of more than 100 million $.


We also provide market report including market size, price comparison, volumes to our business partners.

Regulatory Services

  • 1: We register Bulk Drug (API) formulation with DCGI India.
  • 2: Our Regulatory Department assist in preparing documents required for registration.
  • 3: Registration of over 75 Products in Indian market.
  • 4: Registration of normal and controlled products.
  • 5: We assist in Preparing DMF, Dossier required for registration.

Registration

Basic Documents required for Registration:

  • 1: Good Manufacturing Practice (GMP) Certificate.
  • 2: Drug Master File (DMF).
  • 3: Site Master File (SMF).
  • 4: Free Sales Certificate (FSC) & Others.

Chemicals & Raw Materials Sourcing

With the insight of the industry we understand your concern for the quality. Parth Antibiotics arrange the sourcing of API’s, Intermediate & Chemicals from reputed and established manufacturers whose facilities are approved by regulatory authorities. With our stringent SOP’s, our RA team audits the manufacturers every year which enables us to provide the best. With the increasing demand of Indian Pharmaceutical industry, Parth Antibiotics provide Indenting services to our customers at competitive prices along with perfect documentation and shipments at the required time.

Finished Dosages

Basic Documents required for Registration:

We offer breakthrough finished formulation manufactured under CGMP, WHO & GMP facilities accredited with USFDA, UKHMRA & TGA. We bridge the gap between manufacturer to manufacturer and distributor. As a company driven by science, we are dedicated in improving patient care and quality of life.

600

Projects

200

Suppliers

15,000

Customers & Partners

25

Presence in Countries