Ask Our Experts - Intertek Pharmaceutical Services
Ask Our Experts! - Contact our pharma experts directly with your technical and commercial questions concerning bio/pharmaceutical challenges, regulatory guidance, COVID-19 vaccine, therapeutic or diagnostic development support, and more.
How can we eliminate residual impurities with strategic plans? Learn more in our first Ask Our Expert Q&A:
Mark Parry, Technical Director
Mark has nearly 20 years’ experience working within the pharmaceutical analysis and formulation development industry, with a particular focus on OINDPs. Mostly working in the pre-approval stages, Mark’s background includes extensive experience with product and formulation development for novel and generic products, as well as method development and validation, stability studies, pharmaceutical development activities, and clinical trial manufacturing for a wide range of clients.
Ashleigh Wake, Business Development Director
Ashleigh has held technical and operational management roles in Zeneca, AstraZeneca and Syngenta before joining Intertek. She has a 20 year career as an operational / technical team leader and study director and has specialized in the delivery of GXP studies on biopharma structure, physiochemical and biological activity. She is currently responsible for strategic growth and business development at Intertek’ centre of excellence for biologics characterisation in the UK.
John Todd, Business Development Director
John has held commercial and management roles in several technology companies. He joined Intertek in 2015 and has been responsible for business development, account management, and stewardship of new and existing partnerships. He routinely works with global companies to design tailored outsourcing contracts to meet their technical and commercial needs and has presented at conferences on outsourcing models for the biopharma sector.
CONFERENCE: TIDES EUROPE 2022: Meet us in Vienna
TALK: Medical Device Extractables & Leachables Studies - a Key Part of Biocompatibility Assessments
RDD WORKSHOP: Developing biologics for respiratory delivery
TALK: ID and sensitivity issues during E&L studies
ARTICLE: Glycosylation Analytical Approaches for Antibody Therapeutics
APP NOTE: Rapid Determination of Low/Trace Level Benzene in Pharmaceutical Excipients and Finished Products
ARTICLE: Importance of Aligning a Pharma Audit Scope with the Correct Standard
TALK: mRNA Analytics: Capping Efficiency, Sequencing, Poly-A Tail, dsRNA
TALK: From Extractables to Leachables For Drug Device Combinations
MORE: Comprehensive collection of digital resources
COVID-19 VACCINE OR THERAPEUTIC TESTING & DEVELOPMENT SUPPORT
IMMEDIATE QUESTION? Ask our experts now
FACTSHEET: COVID-19 Vaccine or Therapeutic Testing & Development Outsourcing
ARTICLE: Repurposing Vaccines for Intranasal Development
WEBINAR: Quality Control Strategy for Vaccine Development
WEBINAR: Repurposing Drugs for Inhaled Delivery
eBOOK: Contingency Outsourcing Solutions