How to Source Maraviroc for Pharmaceutical Formulation
Maraviroc (Tablets / Oral solution, 150 mg, 300 mg, 20 mg) is classified under Anti Viral. It is therapeutically aligned with reference brands such as Selzentry (USA), Celsentri (EU). This guide highlights key sourcing factors buyers should consider when procuring high-quality Maraviroc for formulation, R&D, or bulk manufacturing.
Product Overview:
Maraviroc is an antiretroviral medication used in the treatment of HIV-1 infection. It works by blocking the CCR5 co-receptor on human cells, preventing the virus from entering and infecting immune cells. Maraviroc is used in combination with other antiretroviral agents for effective HIV management.
1. Regulatory Compliance & Documentation
Ensure suppliers provide:
- ✔ Valid DMF (Drug Master File)
- ✔ COA (Certificate of Analysis) for each batch
- ✔ GMP, ISO, or ICH Q7 compliance certificates
2. Purity, Grade & Specification Matching
Maraviroc must meet exact grade and purity for your dosage form:
- ✔ USP / EP / JP grade verification
- ✔ Particle size distribution check
- ✔ Residual solvent and heavy metal limits
3. Supplier Reliability & Audit History
- ✔ Positive past audit reports
- ✔ Pharma client references
- ✔ Years of proven API manufacturing experience
4. Commercial Terms: Pricing, MOQ & Flexibility
- ✔ Transparent pricing
- ✔ Pilot batch MOQ flexibility
- ✔ Volume-based discounts
5. Lead Time, Inventory & Logistics
Typical lead time for Maraviroc is 4–6 weeks.
- ✔ Emergency dispatch options
- ✔ Regional warehousing
- ✔ Special storage if needed
6. Formulation Support
- ✔ Technical datasheets
- ✔ Sample availability
- ✔ Stability study support
Conclusion
Sourcing Maraviroc is more than procurement—it’s a strategic partnership. With its tablets / oral solution form and 150 mg, 300 mg, 20 mg specification, choosing a compliant supplier ensures consistent quality and regulatory approval. Prioritize documentation, verify compatibility, and build relationships with transparent, reliable suppliers to secure long-term success.
Next Step: Get expert assistance in sourcing Maraviroc.
Frequently Asked Questions For Sourcing of Maraviroc
What is the typical lead time for Maraviroc?
Lead times range from 4–6 weeks depending on supplier and region.
Is Maraviroc available in multiple grades?
Yes — common grades include USP, EP, and JP. Verify grade suitability for your dosage form before purchase.
Does Maraviroc require special storage?
It should be stored in a cool, dry place away from direct sunlight.
Is a Drug Master File (DMF) available for Maraviroc?
Yes, a DMF is available for regulated markets upon request. It includes detailed quality, manufacturing, and stability data.
Can I request samples or a pilot batch of Maraviroc?
Yes — pilot batches or samples can be arranged for R&D, stability studies, or formulation trials. MOQ may vary based on region and regulatory scope.
What compliance certificates are available for Maraviroc?
Available documentation may include GMP, ISO 9001, ISO 14001, and ICH Q7 certificates, along with CoA, TDS, and stability data.
Is Maraviroc suitable for regulated markets like US/EU?
Yes — compliant with EU/US/WHO GMP standards and available with regulatory support documentation for filings.
Can Maraviroc be used in fixed-dose combinations?
Yes — many formulations support inclusion in FDCs. Compatibility studies and formulation consultation are available on request.
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