The pharmaceutical sector is rapidly expanding in India and worldwide, driven by increasing demand for high-quality medications at affordable rates. In this environment, WHO GMP Certified Third Party Manufacturer producers are becoming increasingly important. WHO-GMP (World Health Organisation – Good Manufacturing Practices) accreditation ensures that pharmaceutical products meet international quality and safety standards. Moreover, various companies seek WHO-GMP-certified producers to ensure that their pharma products fulfil rigorous worldwide safety and quality standards. Hence, this accreditation helps to build confidence between healthcare experts, patients, and overseas customers. Along with this, in today’s times, many nations need this certification for the import of pharmaceutical items. As a result, Indian pharmaceutical businesses that collaborate with certified manufacturers enjoy better access to foreign markets.
Furthermore, third party manufacturing enables pharmaceutical businesses to concentrate on marketing and growth while outsourcing production.
This is possible because leading contract-based production companies only work in high-quality production without heavy investment in infrastructure. In addition, increasing demand for branded and generic medicines is defined as with increased lifestyle illnesses and healthcare awareness, demand for both branded and generic medications is increasing. Thus, various pharmaceutical companies want to work with a WHO-GMP-certified third party manufacturer to preserve product credibility and market presence.
Most importantly, WHO-GMP accreditation lends legitimacy to a manufacturer’s identity, assuring partners and customers of the product’s safety and effectiveness. Hence, the final thought is that the need for GMP-certified third party manufacturers is growing due to their supply of high-quality medications, export support, cost-effective production, and regulatory compliance. This trend is continuing since there is a growing global demand for economical and dependable healthcare solutions.
What types of factors influence you to invest in a genuine third party manufacturer in India
Here are some genuine and important reasons to invest in the best third party manufacturing companies:
Global standard quality assurance:
WHO-GMP accreditation guarantees that pharmaceuticals meet worldwide quality and safety requirements. Hence, particularity increases acceptance in both home and export markets.
Regulatory compliance and easy approvals:
Ready pharma products from those facilities face fewer challenges with DCGI, DCSCO, and even worldwide regulatory agencies. Hence, this lowers the chance of rejection and delays.
High market credibility:
Partnering with a qualified pharmaceutical third party manufacturing company improves your brand’s image and fosters strong confidence among physicians, distributors, and patients.
Access to advanced manufacturing technology:
If you invest in the top organisations that utilise cutting-edge infrastructure, computerised systems, and rigorous hygiene standards, you can get consistent quality and cost-effectiveness in each pharmacy product order.
Wide export opportunities:
GMP accreditation qualifies products for supply in worldwide markets. Hence, this broadens your business’s reach outside India.
Reduced operational burden:
Leading third party manufacturing enables you to concentrate on marketing and distribution while professionals manage formulation, production, and compliance.
Scalability and cost efficiency:
As pharma product manufacturing investors, you can gain various benefits like economies of scale and cheaper manufacturing costs. Also, you can get the ability to scale up production without a significant capital commitment.
Important working processes in the leading third party manufacturing company
Here are the important and major key procedures of our third party pharma manufacturing company to ensure high-quality and compliant production:
Requirement and quotation finalisation:
In the beginning, we ensure that the customer shares product specifications (formulation, strength, and packaging). Here, we also deliver them a quote that includes the cost, minimum order quantity (MOQ), and timetable.
Documentation and regulation approval:
Submission of required paperwork, such as a drug license, GST, and company profile. Also, we ensure compliance with WHO GMP criteria and create product dossiers.
Product development and composition approval:
The r&d team develops formulations based on customer specifications. After this, the composition and package designs are finalised with customer approval.
Raw material procurement:
We ensure that only high-quality APIs and excipients are obtained from recognised vendors. Then we also ensure that before beginning manufacturing, each material is thoroughly inspected for quality.
Batch manufacturing process:
In our company, manufacturing takes place under controlled settings in accordance with WHO-GMP guidelines. After this, weighing, mixing, granulation, compression/capsule filling, coating, and packing (depending on dosage type) are the important steps that are part of our manufacturing processes.
Quality control and assurance:
We do various testing of both in-process and completed products that take place in properly equipped labs. Moreover, our manufacturing company ensures that each batch is tested for stability, purity, and potency before being released.
Packaging & labelling:
In the end, the time comes for the packing, and here our products are packaged in WHO-GMP-compliant facilities. Even with this, all regulatory data, such as the batch number, MRP, and manufacturing/expiry date, are properly labelled.
Conclusion
Finally, the discussion on this topic is completed, and we have deeply discussed that certified manufacturing facilities of the pharma products are very important and beneficial for the pharma companies. Along with this, Intelicure Lifescience is one of the leading brands that offer the most genuine manufacturing of the pharma items. Thus, the search for the genuine WHO-GMP-certified third party manufacturer in the country should get our services now.
FAQs
Q: Why would a pharmaceutical company employ third-party manufacturing?
A: Pharmaceutical third party manufacturing services help reduce the burden of infrastructure, investment, and regulatory compliance. This allows companies to focus more on marketing, branding, and sales, while experienced manufacturers manage production, quality assurance, and timely delivery.
Q: What paperwork is important to commence third-party manufacturing?
A: The commonly required documents include:
- Valid Drug License (DL) number
- GST Registration Certificate
- Company PAN Card
- Marketing and Corporate Profile
- Product composition details
- Packaging material artwork/requirements