Salvat - CDMO/CMO

A CMO is a contract partner focused on manufacturing execution under GMP. For drug products this often includes tech transfer, validation, routine manufacturing, packaging, and supply continuity.

Typical CMO services include tech transfer, GMP manufacturing, validation support, packaging, QC testing where applicable, and batch release workflows aligned to target markets.

Choose a CMO when the formulation and process are largely established and you need manufacturing capacity and reliable supply. Choose CDMO scope when you still need development work (formulation/process development/method development).

Start with dosage-form fit (sterile vs non-sterile, device needs), then filter by certifications and target markets (FDA/EMA), capacity, and realistic timelines. This directory is built for that workflow.

Include dosage form, stage, batch sizes and annual demand estimate, target markets, packaging format, cold chain needs, and key quality expectations. Clear inputs lead to faster, more accurate proposals.

Fill-finish is the step where drug product is filled into final containers (vials, syringes, pens) and packaged. Facility design, sterility assurance, and packaging components often drive timelines and feasibility.

Confirm market experience (FDA/EMA), inspectable quality systems (deviations/CAPA, change control), documentation readiness, and whether the specific facility/suites are in-scope for your product type.

Capacity windows, packaging component lead times, validation strategy, and analytical/QC readiness are common drivers. Sterile injectables and complex packaging formats typically require longer planning.

Many do, but packaging capability is not universal. Validate line compatibility, serialization requirements, component sourcing responsibilities, and release workflows.

Custom CMO services usually mean tailored packaging, special handling (cold chain), device requirements, or non-standard batch strategies. Use them when your product needs go beyond a standard manufacturing run.

Compare on dosage-form fit, proven experience, certifications and market history, QA maturity, realistic lead times, and packaging capabilities. Use filters first, then deep-dive with RFQs.

Often not for a high-level brief. Most buyers share a concise scope first and sign an NDA when detailed transfer documents are needed.

Manual search is slow and inconsistent. A directory approach lets you compare providers by the same criteria (dosage form, certifications, markets, scale), so you can shortlist faster and avoid contacting mismatched suppliers.

Contract manufacturing services usually focus on execution and supply. CDMO services typically include development work alongside manufacturing. For drug product, choose based on whether you need development or mainly manufacturing capacity.

Yes. If you’re unsure, use the open inquiry option: one message with your requirements routed to relevant CMOs, helping you compare responses without repeating the same work.

“Pharma contract fillers” usually refers to CMOs that perform fill-finish operations, especially for sterile injectables. Verify container formats, aseptic capabilities, and packaging lines for your product.