Ventalys supports select CDMO and custom manufacturing requirements across formulations, solid and semi-solid dosages, liquids, and suppositories. Through qualified manufacturing relationships, we help pharmaceutical companies, distributors, and finished-dosage manufacturers review practical production pathways for commercial, clinical, and development-stage programs.
Our CDMO capabilities include formulation support, dosage development, scale-up coordination, manufacturing review, documentation support, and commercial supply assistance where available.
Ventalys supports formulation-focused programs for pharmaceutical products that require practical development, manufacturing review, and documentation coordination. This may include product-specific formulation assessment, excipient compatibility review, process considerations, and manufacturing pathway support.
Ventalys can support requirements involving tablets, capsules, powders, granules, creams, ointments, gels, and other solid or semi-solid dosage formats, subject to product fit, facility capability, documentation requirements, and customer approval.
Ventalys supports liquid dosage requirements where available, including oral liquids, suspensions, solutions, and other liquid-format pharmaceutical products. Each project is reviewed based on formulation complexity, batch size, stability, packaging, documentation, and target market requirements.
Ventalys can help review select suppository manufacturing requirements, including formulation, base selection, manufacturing feasibility, packaging considerations, and documentation support for customer review.