Respiratory syncytial virus mRNA vaccine bulk supplier for pharma manufacturers

Respiratory Syncytial Virus Mrna Vaccine Suppliers & Bulk Manufacturers

Available Forms: injection (prefilled syringe)

Available Strengths: 0.5 mL

Reference Brands: mRESVIA (USA/EU)

Category: Vaccines

mRESVIA is an mRNA vaccine designed to protect adults against lower respiratory tract disease (LRTD) caused by RSV. It works by instructing the body to produce a harmless RSV F protein fragment, triggering immune protection. Administered as a single 0.5 mL intramuscular injection, it is indicated for adults 60 years and older and adults 18–59 at increased risk. It is the first non‑COVID‑19 mRNA vaccine approved in several regions. Common side effects include pain at injection site, fatigue, headache, and muscle aches. Respiratory syncytial virus mRNA vaccine is available in injection (prefilled syringe) and strengths such as 0.5 mL. Sourced from GMP-certified and ISO-compliant manufacturers, this API meets global pharmacopeia standards (USP/EP/JP as applicable). Ideal for pharmaceutical formulation and commercial manufacturing, Respiratory syncytial virus mRNA vaccine is supplied in bulk quantities with complete regulatory support including DMF, COA, and MSDS.

Technical Specifications & Supply Details
Lead Time 7 to 60 days (depending on batch size & schedule)
MOQ As per manufacturer’s batch size
COA Available with every batch
Regulatory Dossier / DMF Available upon request
Export Documentation FSC, COA, Manufacturing License, Product Permission
Standards IP, BP, USP
Certifications WHO-GMP, EU-GMP, USFDA (as applicable)

Respiratory syncytial virus mRNA vaccine can be exported to over 30 countries across Asia, Africa, Europe, and Latin America. Flexible packaging, competitive pricing, and a verified supplier network make Pharmatradz a trusted sourcing partner for pharmaceutical companies and contract manufacturers worldwide.

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📘 Sourcing Guide

Product Description:

mRESVIA is a messenger RNA (mRNA) vaccine developed to actively immunize adults against lower respiratory tract disease (LRTD) caused by Respiratory Syncytial Virus (RSV), which can cause severe lung infections, particularly in older adults and at-risk populations. The vaccine contains nucleoside-modified mRNA (mRNA‑1345) encoding a stabilized RSV F glycoprotein in its prefusion form. When administered as a 0.5 mL intramuscular injection, the mRNA instructs the recipient’s cells to produce the RSV F protein fragment, stimulating the immune system to generate protective antibodies without using live virus. mRESVIA is indicated for adults 60 years and older and adults 18 through 59 who are at increased risk of severe RSV disease. The vaccine may cause mild to moderate side effects such as pain at the injection site, fatigue, headache, muscle pain, joint pain, and chills. Its approval marks one of the first uses of mRNA technology for a disease other than COVID‑19, demonstrating the potential of mRNA vaccines to prevent other viral illnesses in adults.

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Frequently Asked Questions

mRESVIA is used to actively immunize adults against

mRESVIA is an mRNA vaccine formulated with

The trade name of this RSV mRNA vaccine is

mRESVIA is manufactured by

The generic name of mRESVIA is

The brand name of the RSV mRNA vaccine is

mRESVIA is manufactured under regulated pharmaceutical conditions by

Yes, Respiratory syncytial virus mRNA vaccine is available with DMF and other regulatory documents such as COA and MSDS. These can be provided upon request for qualified buyers.

Absolutely. Sample requests are accepted for formulation trials and quality checks. Please submit an enquiry to initiate the process.

Our manufacturing partners are GMP-certified and comply with ISO and WHO standards, ensuring global quality benchmarks.

Lead times vary based on quantity and destination, but most orders are fulfilled within 1–3 weeks. Express shipping options are available.

Yes, Respiratory syncytial virus mRNA vaccine is exported to over 30 countries across Asia, Africa, Europe, and Latin America. We support documentation for customs and regulatory clearance.

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