ADVENT provides a wide variety of services to the Biologics and Pharmaceutical industry. The services range from process development and technology transfer to engineering design, commissioning, qualification, and validation (CQV), and Pre-approval Inspection (PAI) Readiness. ADVENT’s talented and experienced team of professionals has delivered these services throughout the U.S., Europe, and Asia to the biopharmaceutical industry’s leading firms.
Monoclonal Antibodies (mAb)
Solid Oral Dose
Trans Dermal Patch
Qualification and Validation Services
We are well-versed in developing and implementing risk-based approaches to process validation
Process Development Services
ADVENT’s process development experience comes from supporting the cGMP manufacturing of bulk drug substances (BDS) for many clients.
ADVENT provides a wide array of engineering services to support every phase of the “GEP Lifecycle” from planning for new products to retirement of equipment.
Project Management Services
We offer integrated project management services and methodology, supported and reflected by our experience and policies.
Training modules filled with cogent, up-to-date information to enhance the knowledge base of personnel involved with validation, qualification, engineering, and manufacturing.