3rd Party Manufacturing Pharmaceuticals in India | Docrix Healthcare

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3RD PARTY MANUFACTURING PHARMACEUTICALS IN
INDIA
docrix.in
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What Is A Third Party Pharmaceutical
Manufacturer?
A third party pharmaceutical manufacturer is a
company that produces drugs on behalf of another
company. These companies may provide services
such as compounding, formulating, packaging,
labeling, and distributing drugs. Third party
manufacturers ensure quality control and prompt
delivery of pharmaceutical products. A
fourth-party logistics provider is a company
that assists pharma companies in moving their
products from the point of manufacture to the
point of use sometimes called fulfillment
services.
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About Us
Are you searching for the best business if you
are unsure which 3rd Party Manufacturing
Pharmaceuticals in India will be best for you?
Then, all of the looking and working out has come
to an end. One of the biggest and finest
manufacturers of Third Party Pharmaceuticals in
India is Docrix Healthcare. As a reputable
business, we are dedicated to providing you with
the highest quality medical treatment. We
accomplish this by creating the ideal goods for
the ideal markets, which promotes the expansion
of your company.
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Advantages Of Partnering With Third Party
Pharmaceutical Manufacturers In India
3 Timely delivery India's third party
pharmaceutical manufacturers are renowned for
their prompt product distribution, ensuring
that the goods reach the market on schedule.
1 Cost-Effective Given the abundance of skilled
labor and cheap cost of production, India is a
very cost-effective place to manufacture
pharmaceuticals for third parties.
5 Regulatory compliance Indian third-party
pharmaceutical producers adhere to a variety of
ethical and legal standards as set forth by the
government of India.
2 Flexibility India's third party pharmaceutical
producers provide a high level of flexibility
in terms of production capability packaging
choices.
4 High-quality standards Indian pharmaceutical
companies that manufacture for others follow
stringent quality standards.
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Quality
All aspects of the production process, from the
sourcing of raw materials to the packaging and
labeling, are subject to stringent quality
control standards.
Expertise Our staff is made up of highly
qualified and seasoned individuals who are
knowledgeable about the most recent
manufacturing techniques and technologies.
Why Choose Us?
Affordability We can manufacture pharmaceutical
products of the highest caliber at competitive
costs thanks to our efficient manufacturing
procedures.
Flexibility When it comes to manufacturing
capability, product selection, and packaging
choices, we provide a high level of flexibility.
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Business Plan
Create a business plan that explains your goals,
your target market, and the goods you want to
produce.

• The Complete Process For Establishing A Third
  Party Manufacturing Company In India

Choose a Location Considering the accessibility
of raw materials, infrastructure, logistics
will help you choose an appropriate site for your
manufacturing facility. Obtain Licenses Obtain
the required state and federal licenses
permits, such as a drug license, a registration
for the (GST), a company registration. Manufact
uring Site Create a manufacturing facility with
the necessary utilities, machinery, equipment
to satisfy GMP WHO standards.
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Raw Material Procurement
Obtain basic materials from trustworthy vendors
who adhere to quality standards and laws.
Production Begin manufacturing pharmaceutical
goods under the guidance of trained and
knowledgeable staff.
Quality Control Establish a strong quality
control procedure that guarantees the
goods' efficacy, safety, and quality.
Packaging Labeling The products must be
packaged and labeled in accordance with
regulatory requirements, the packaging must be
tamper-proof contain all required information,
including dosage, ingredients, an expiration
date.
Distribution Through a network of distributors or
agreements for contract manufacturing with other
businesses, distribute the goods to the market.
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Drug License
Pharmaceutical product production in India
requires a drug license. The State Drugs Control
Department issues drug licenses, so it's crucial
to send the application with all required
paperwork.

• Documents Required For 3rd Party Manufacturing
  Pharmaceuticals In India

Company Registration The Memorandum of
Association (MOA), Articles of Association
(AOA), and Certificate of Incorporation are the
documents required for business
registration. Product Approval The Drug
Controller General of India (DCGI) must be
consulted and given final clearance before the
product can be released.
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GST Registration
Any company in India with an annual revenue of
over Rs. 40 lakhs must register for GST. PAN
cards, location proofs, and information about
bank accounts are among the paperwork needed for
GST registration.

• Quality Control Documents
• SOPs for quality control, laboratory test
  results, and validation reports are all included
  in the quality control papers.
• Manufacturing Site Approval
• Good production Practices (GMP) and WHO
  guidelines should be followed by the production
  facility.
• Contract Manufacturing Agreement
• The terms conditions of the manufacturing deal
  between the third party manufacturer the brand
  owner are set forth in the contract
  manufacturing agreement, which is a legal
  document.

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Contact Us
91-172-4111127 www.docrix.in info_at_docrix.in Plot
14, Industrial Area, Phase 2, Panchkula, Haryana
134113