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Providing expert support to the external manufacturing operations department of a Major Pharma during the technology transfer of a blockbuster product from in-house manufacturing to a third party CMO

Objective Oversight of the technology transfer of a blockbuster status injectable product from in-house production to a qualified contract manufacturing organization while changing from a

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Compliance oversight of the process development and validation of a Biosimilar active ingredient manufacturing at a CMO on behalf of the sponsor biopharmaceutical company

Objective Providing GMP compliance oversight to the process scaling-up and validation of a complex biosimilar manufacturing by a qualified contract manufacturing organization, up to Marketing

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Design and implementation of a complete supply chain solution for a small research-based biotech company

Objective Selecting and qualifying a primary and secondary manufacturing service provider for the transfer of the in-house developed biotech drug candidate, suitable for supplying clinical-grade

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Implementation of a GMP-compliant internal drug substance manufacturing capability for a startup biotech

Objective Creating an in-house GMP-compliant manufacturing capability for a small biotech startup in order to fully leverage the technological platform developed by the firm Outcome

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Technical expert support for the transfer of a portfolio of mature injectable products from one CMO (liquid in vials) to another CMO (solution in pre-filled syringes)

Objective Due to the discontinuation of the related range of activities by the historical CMO, transfer of a portfolio of injectable emergency medicines to another

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Interim management of the sterile products development department of a leading CMO

Objective Act as interim head of a fully integrated PDS unit within the premises of a leading European sterile manufacturing CMO Outcome P&L level management

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Point person for the FDA inspection of a fine chemical manufacturing site

Objective Prepare and handle the FDA inspection of a fine chemicals manufacturing site, where one of the site legacy products had been the object of

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Person-in-Plant for a leading innovative US biotech firm at their main European contract manufacturing partner

Objective Provide technical and compliance support on-site during critical steps of the pre-PPQ and PPQ runs of a complex and highly innovative synthetic active pharmaceutical

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CMC expert support to an innovative drug development program (drug substance and drug product) for a mid-sized established traditional pharmaceutical group

Objective Provide scientific, manufacturing and compliance support to the pharmaceutical development group of a traditional mid-sized pharmaceutical company developing an innovative complex synthetic molecule formulated

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Complete CMC and quality oversight responsibility for a very small biotech startup company, with no internal technical operations capability or experience

Objective Manage the complete network of external service providers for drug substance and drug product process development and manufacturing as well as analytical services; drafting

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Expert witness in a patent litigation on behalf of the originator

Objective Provide scientific and industrial rationale for the innovative character of the patent claims challenged by a potential generic competitor Outcome Writing of several expert

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Due diligence addressing the technical operations capabilities of the target company in a M&A situation

Objective Provide a detailed business case for the operational capability (including estimated profitability) of a contract manufacturing organization on behalf of a pharmaceutical group looking

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Marble Pharma Consult 2019