Contract Manufacturing & Third-Party Manufacturing in India
Our facilities Accredited & Complied
With WHO-GMP standards, We offer seamless service from the Plant registration to Development/Registration, and Commercialisation of the products globally
40+
Exporting Countries
12+
Years Of Experience
500+
Clients Globally
2000+
Product Lines
550+
Ready Dossiers
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Contract manufacturing and third-party manufacturing are related, but they are not the same.
Contract manufacturing means full production in accordance with your specifications.
Third-party manufacturing focuses on producing products under your brand name. Actiza provides both options based on your business needs.
Actiza Pharmaceutical has strong experience in this field. With over 12 years of experience, we serve clients in more than 40 countries.
Our facilities are WHO-GMP certified. We produce both APIs and finished formulations, giving you complete supply support.
Whether you want to scale a product or enter new markets, choosing the right partner is important.
Get a Quote or connect with our team today.
Contract Manufacturing vs Third-Party Manufacturing – What’s the Difference?
Both models support pharmaceutical outsourcing, but they differ in control, ownership, and responsibility. Your choice depends on your business goals.
In contract manufacturing, you own the formulation or molecule. Actiza produces it based on your specifications. This works best for businesses with their own R&D or products.
In third-party manufacturing, Actiza provides ready-made formulations. You sell them under your own brand. This helps you enter the market faster without investing in R&D.
Key Differences at a Glance
| Parameter | Contract Manufacturing | Third Party Manufacturing |
| Ownership of Formula | Client-owned | Actiza-owned |
| Branding | Client brand | Client brand |
| Regulatory Responsibility | Shared / client-led | Actiza-supported |
| Ideal For | Companies with IP or formulations | Companies seeking ready products |
Actiza seamlessly operates under both models, based on your requirements.
Our Contract & Third-Party Manufacturing Services
Actiza is a fully integrated manufacturing system. Everything is handled under one roof, starting with APIs, Advanced Intermediates and finishing with products.
This enhances quality, accelerates schedules and minimises coordination problems.
Finished Formulation Manufacturing
Actiza produces many types of finished dosage forms. Our facilities support 25+ dosage formats and 2000+ products.
This assists you in achieving a broad product line with a single partner.
We manufacture:
All products follow strict WHO-GMP standards for safety and consistency.
API & Advanced Intermediates Manufacturing
Actiza has deep expertise in API & Advance Intermediates manufacturing. We do bulk production, as well as custom synthesis and advanced intermediates.
All API and Advanced Intermediates manufacturing is by cGMP, high-purity, and compliance standards.
Key strengths:
You can source APIs and finished products from one place.
Private Label & White Label Manufacturing
Actiza lets you have complete control of your brand. We produce goods under your brand name and are prepared to sell them in the market.
We support:
This model works well if you want to enter new markets or expand your product range quickly.
Now that we have covered branding, let’s move to end-to-end support.
End-to-End Manufacturing
Actiza deals with the entire manufacturing process. This lessens your workload.
Our process includes:
This ensures a seamless production flow.
Therapeutic Areas We Cover for Contract & Third-Party Manufacturing
Actiza has a broad range of therapeutics. This assists you in creating a robust and diversified product portfolio.
We cover:
All therapeutic categories are available in both API and finished formulation formats.
Our Contract & Third Party Manufacturing Process – Step by Step
Actiza has a straightforward and transparent production procedure. Each of the steps will be designed to sustain quality, adhere to rules and provide timely delivery of products in the global markets.
Requirement Analysis & Consultation
We get to know about your product, target market and business objectives first. This assists us in making decisions on how to produce your product in the most efficient manner.
Feasibility & Regulatory Assessment
Our staff verifies that the product can be manufactured correctly and in accordance with the necessary regulations. This will prevent procrastination or denial in the future.
Sourcing and Quality Tests of Raw Materials.
We receive raw materials and APIs from reliable suppliers. Any batch is vigorously tested.
Pilot Batch Development
We produce a pilot batch to be tested and approved. This ensures that the product is stable, consistent and is ready to be produced in large quantities.
Preparation of Regulatory Filing and Dossier
We assemble all the documents needed to be approved. These records adhere to the regulations in every nation.
Commercial Scale Manufacturing
Manufacturing is done in WHO-GMP-certified facilities. All steps are closely checked to keep quality and efficiency high.
Quality Control and QA Testing.
All the batches are in-house tested. Each stage is checked in terms of quality to be safe and consistent.
Packaging, Warehousing & Global Dispatch
Products are filled according to the necessary standards. We are also in charge of storage and delivery on time throughout the world.
GMP-Certified and Globally Compliant Manufacturing
At Actiza, quality and compliance come first. Our systems are built to meet global standards and deliver consistent product quality.
We have multiple certifications and approvals:
All our processes follow ICH guidelines. This helps our products get accepted in both regulated and semi-regulated markets.
We also offer strong regulatory support:
Our regulatory support makes it easier for you to enter new markets:
This complete system helps reduce approval time and ensures the same quality in every batch.
Why Partner with Actiza for Contract & Third Party Manufacturing?
Selecting an appropriate manufacturing partner influences the quality of your product, speed and marketing success.
Actiza is experienced, with a high capacity and regulatory knowledge to assist pharmaceutical businesses across the globe.
12+ years of experience in APIs and formulations
Single source of APIs, intermediates and finished products
Exporting to 40+ countries with 500+ clients worldwide
Competitive pricing without compromising quality
Dedicated project manager for every client
Automatic packaging of 80%+ to improve speed and accuracy
Strong in-house R&D with pilot batch capabilities
Complete regulatory assistance, such as dossiers and approvals
This entire strategy assists in saving time, cost management, and ensuring that the quality of goods remains the same in all the markets.
Frequently Asked Questions About Contract & Third-Party Manufacturing
Q 1. What is the difference between contract manufacturing and third-party manufacturing in pharma?
Contract manufacturing involves the production of your formulation or IP. Third-party manufacturing utilises ready formulations created by Actiza, which are sold under your brand.
Q 2. Does Actiza manufacture APIs along with finished formulations?
Yes. Actiza offers API manufacturing and finished products. This guarantees improved control and dependability of supply.
Q 3. What is the minimum order quantity for contract or third-party manufacturing?
MOQ is dependent on the dosage type and the product. We have dynamic solutions according to your requirements.
Q 4. Do you provide regulatory and dossier support for new markets?
Yes. We assist in preparing dossiers, submitting them, and achieving compliance by country in order to make it easier to enter the market.
Q 5. How long does it take to begin production after signing an agreement?
Timelines will be based on the product and approvals. Production in most instances begins in several weeks, once documentation and checks are accomplished.
Start Your Contract or Third-Party Manufacturing Partnership with Actiza
Actiza offers a single location for a complete manufacturing solution. We supply the accuracy and flexibility of contract and third-party production, whether in the form of APIs and intermediates or finished products.
Having WHO-GMP certified plants and representation in 40+ countries, we can offer quality you can trust and scale you can rely on.
Ready to get started?
Get in touch with our team now by filling out our form, calling us or emailing us to talk about your needs.