Demonstrating a search for a CDMO | Pharma Services Hub

Selecting a CDMO for a Phase 1 small-molecule programme? Watch a live walkthrough of the Pharma Services Hub CDMO sector search. In this demo, Mike Frodsham takes you inside the Pharma Services Hub platform and runs a real outsourced-side search for a contract development and manufacturing organisation (CDMO). Using a representative Phase 1 capsule project as the worked example, Mike shows exactly how the platform translates your project requirements into a relevance-ranked shortlist of qualified service providers, and how to issue a structured RFP without scattergun outreach. You will see how to: Set the project background (molecule type, route of administration, therapeutic indication, project type and phase of development) so service providers can quickly assess fit. Capture API handling considerations, including potency, oxygen and light sensitivity, alongside licence and quality requirements such as GMP and MIA. Specify technical service needs across drug substance, drug product development and GMP manufacturing, drilling down to analytical method development, in vitro dissolution, related substances by HPLC, micro and moisture content. Define formulation strategy where bioavailability enhancement is required, including amorphous solid dispersion and lipid delivery considerations, plus downstream processes such as spray drying and powder blending. Review a relevance-matched provider list, read company profiles, partnership questions and client testimonials, then select up to five providers for an RFP. Generate, customise and issue the RFP. including CDA/NDA attachment, and track viewership, interest and response times from a single dashboard. The Pharma Services Hub CDMO sector is engineered to remove the friction from outsourcing. By forcing technical clarity at the front end, the platform protects your time and the service provider's, and accelerates the path from initial inquiry to contracted engagement. The same workflow applies across every sector on the platform. If you are evaluating CDMO partners for drug substance, drug product or GMP manufacturing, this walkthrough is the fastest way to understand what the platform does on your behalf. 🧪 Start your CDMO Search: https://www.pharmaserviceshub.com/ 📈 View Platform Features: https://www.pharmaserviceshub.com/features 🔗 Follow us on LinkedIn: https://www.linkedin.com/company/pharma-se... 🔎 Start your search: https://app.pharmaserviceshub.com/Identity... #CDMO #PharmaOutsourcing #DrugDevelopment #PharmaServicesHub #ContractManufacturing 00:00 Introduction: the demo begins 00:34 Selecting the CDMO sector 00:54 Project background: small molecule, capsule, Phase 1 02:00 Therapeutic indication and project type 02:55 Timeline, API handling and potency considerations 03:53 Licence requirements and quality standards 04:28 Specifying technical services 05:35 Analytical development and characterisation 06:26 Drug product formulation and bioavailability enhancement 07:35 Dosage form: capsule selection 08:08 GMP manufacturing, stability and QP release 09:18 Process details: spray drying and powder blending 10:14 Naming the search and reviewing matched providers 10:46 Reading site profiles and partnership questions 12:12 Selecting providers for RFP 13:31 Building and customising the RFP 14:29 Adding the CDA/NDA and sending 15:03 Tracking inquiries and provider responses 16:25 Closing summary