How to Source Maribavir for Pharmaceutical Formulation
Maribavir (Tablets, 200 mg) is classified under Anti Viral. It is therapeutically aligned with reference brands such as Livtencity (USA/EU). This guide highlights key sourcing factors buyers should consider when procuring high-quality Maribavir for formulation, R&D, or bulk manufacturing.
Product Overview:
Maribavir (Livtencity) is an antiviral used to treat cytomegalovirus (CMV) infection in patients who have had an organ or stem-cell transplant and whose CMV infection is resistant or refractory to standard treatments. It works by inhibiting the viral protein kinase pUL97, preventing CMV DNA replication, encapsidation, and nuclear egress, thereby stopping the virus from multiplying.
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
Maribavir 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 Maribavir 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 Maribavir is more than procurement—it’s a strategic partnership. With its tablets form and 200 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 Maribavir.
Frequently Asked Questions For Sourcing of Maribavir
What is the typical lead time for Maribavir?
Lead times range from 4–6 weeks depending on supplier and region.
Is Maribavir available in multiple grades?
Yes — common grades include USP, EP, and JP. Verify grade suitability for your dosage form before purchase.
Does Maribavir require special storage?
It should be stored in a cool, dry place away from direct sunlight.
Is a Drug Master File (DMF) available for Maribavir?
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 Maribavir?
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 Maribavir?
Available documentation may include GMP, ISO 9001, ISO 14001, and ICH Q7 certificates, along with CoA, TDS, and stability data.
Is Maribavir suitable for regulated markets like US/EU?
Yes — compliant with EU/US/WHO GMP standards and available with regulatory support documentation for filings.
Can Maribavir 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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