PHARMACEUTICAL EXPORTS
- Medesta headquartered in Mumbai is one of the leading exporter and manufacturer of finished pharmaceutical formulations
- State of the art WHO - GMP manufacturing facility for finished pharmaceutical formulations
- Certification of Countries: Fda – Afghanistan, Moh – Cambodia, Fda – Georgia, Dpm- Ivory Coast ,Fda – Nepal, Moh- Myanmar, Nafdac- Nigeria, Csb – Vietnam, Fda – Srilanka, Fda – Sharjah(UAE) , Ppb – Kenya, Tmda – Tanzania, Fda – Togo, Nda – Uganda, Fda –Uzbekistan, Zfdb – Zanzibar, Jfda – Jordan, Fda- Philliphines, Fmhaca – Ethiopia, Moh –Kazakhstan, Pra – Zambia, Jmpb – Sudan, Fda – Ghana, Moh – Libya, Moh – Yemen, Digemid –Peru, Mcaz- Zimbabwe.
- We have full range of data for acceptance of Dossiers for countries around the Globe. CTD Dossier availability for a wide range of products.
- GEOGRAPHICAL PRESENCE - We have a strong presence in Africa, CIS markets and LATAM markets with a vision to set up own marketing & promotions team in these countries.
We are a strategic partner to overseas customers for local government tenders. We have successfully supplied in government tenders of CMAM (Mozambique), RBC (Rwanda), NIPDEC(Trinidad & Tobago), NDSO (Lesotho), etc, providing value addition to our partners across the Globe.
Medesta has a team of professionals who have in-depth knowledge of the International pharmaceutical market as they have been there in the industry for more than a decade. The integration of this professional talent ascertains our service in terms of speed, accuracy & efficacy.
Commitment to Quality- Quality is at the core of everything we do. From the products we offer to the services we provide, we uphold the highest standards in the industry. Our relentless dedication to improvement ensures that our quality remains unrivaled.
Customer-Centric Approach- Our customers are not just clients; they are our partners in success. We prioritize building long-term, mutually beneficial relationships, where exceeding expectations is the norm.
Affordable Pricing and Customization- Making high-quality products accessible is a fundamental aspect of our ethos. We offer a diverse range of products, each available in multiple options to cater to various needs and budgets. Our commitment to sustainability extends to ensuring affordability without compromising on quality.
Innovation for Tomorrow- We continuously seek new solutions to address evolving challenges, particularly in healthcare. Our dedicated research efforts aim to introduce innovative products that meet unmet clinical needs, driving positive change in the industry.
Regulatory Excellence- Ensuring compliance and adherence to regulatory standards is paramount. Our experienced team manages the technical documentation and regulatory requirements seamlessly, facilitating swift product registrations in different countries. With a global network of associates, we navigate regulatory landscapes with precision and efficiency.
We meticulously build quality into our products at each step right from vendor development , raw material in process QC to finished process QC.
Use of modern equipment AAS, MMR, HPTLC, GC, FTIR UV VISUAL & SPECTRO PHOTO METER to achieve highest standard of quality finished products.
During our engrossed presence in the industry, we had the privilege to assist several International regulatory audits. This has enriched us with pertinent knowledge about International audits. We utilize this knowledge to assist other manufacturers to get their manufacturing facility audited by various regulatory authorities across the globe.
To achieve our goals, we are committed to continuous personal interaction with our international suppliers and our clients
Medesta’s core strengths
Transparency & Integrity
- At Medesta we find transparency & integrity are the best policy and hence communicate transparently & with full integrity to our entire valued associates at all levels of the transaction. This not only helps us in nullifying the conflicts but also assures us of the strong business bonding with our partners.
Our warriors
- We have a series of gems that help us shine at all levels of our services because of their commitment level. Most of our staff is from the pharmaceutical background & has been serving the pharma industry for a considerable period.
- Being into Lifecare industry, we understand our products save and render new life to ailing human being thus we take extra care during the manufacturing process by complying to various quality standards. We are pledged to make affordable and best quality products by adhering to international standards.
- Movement of goods is the essence of pharma business as the products require strict temperature regulation & careful handling of products which are packed in glass. Qualified team of logistics professionals with wide experience in handling shipments by sea and air assigned for different countries across the globe.
FAQ
Q1. What are pharmaceutical product exports?
Pharmaceutical product exports involve the international trade of medications, medical devices, vaccines, and other healthcare-related products across different countries.
Q2. What regulations govern pharmaceutical product exports?
Pharmaceutical exports are subject to strict regulations imposed by both the exporting and importing countries, including quality standards, labeling requirements, packaging guidelines, and documentation compliance.
Q3. What is Good Manufacturing Practice (GMP)?
GMP is a set of quality assurance guidelines and practices that ensure pharmaceutical products are consistently produced and controlled to meet the required quality standards.
Q4. How do I obtain the necessary export licenses for pharmaceutical products?
Export licenses for pharmaceutical products are usually obtained from the relevant government agencies. These licenses ensure compliance with regulations and allow the legal export of specific products.
Q5. What documentation is required for pharmaceutical product exports?
Documentation might include certificates of analysis, certificates of origin, packaging information, labeling details, product registration documents, and other regulatory paperwork.
Q6. What role does intellectual property (IP) play in pharmaceutical exports?
Protecting intellectual property is crucial in pharmaceutical exports to prevent unauthorized production and sale of patented medications. This involves understanding and adhering to patent and copyright laws.
Pharmaceutical product exports involve the international trade of medications, medical devices, vaccines, and other healthcare-related products across different countries.
Q2. What regulations govern pharmaceutical product exports?
Pharmaceutical exports are subject to strict regulations imposed by both the exporting and importing countries, including quality standards, labeling requirements, packaging guidelines, and documentation compliance.
Q3. What is Good Manufacturing Practice (GMP)?
GMP is a set of quality assurance guidelines and practices that ensure pharmaceutical products are consistently produced and controlled to meet the required quality standards.
Q4. How do I obtain the necessary export licenses for pharmaceutical products?
Export licenses for pharmaceutical products are usually obtained from the relevant government agencies. These licenses ensure compliance with regulations and allow the legal export of specific products.
Q5. What documentation is required for pharmaceutical product exports?
Documentation might include certificates of analysis, certificates of origin, packaging information, labeling details, product registration documents, and other regulatory paperwork.
Q6. What role does intellectual property (IP) play in pharmaceutical exports?
Protecting intellectual property is crucial in pharmaceutical exports to prevent unauthorized production and sale of patented medications. This involves understanding and adhering to patent and copyright laws.