• Catalent Webinar: Small molecule orphan drugs: Status quo, Challenges, and Perspectives

    Catalent Webinar: Small molecule orphan drugs: Status quo, Challenges, and Perspectives

    Join Evelyn Kelly at Catalent’s webinar: Small molecule orphan drugs: Status quo, Challenges, and Perspectives February 07, 2023. 11:00am EST/4.00pm IST   Orphan Drug Consulting’s Evelyn Kelly will be a guest speaker on Catalent’s webinar: Small molecule orphan drugs: Status quo, Challenges, and Perspectives on February 7, 2023, at 11.00 am EST/4.00 pm IST.  In

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  • J.P. Morgan Healthcare Week 2023

    J.P. Morgan Healthcare Week 2023

    January 9th-12th, 2023 CEO and Founder of Orphan Drug Consulting, Evelyn Kelly, will be visiting San Francisco for J.P. Morgan week in January 2023. Widely considered one of the most prominent events in the biotech and pharma industry, Evelyn is excited to meet fellow industry members in San Francisco during this week. Reach out below

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  • Webinar: Good Manufacturing Practices: Annex 21

    Webinar: Good Manufacturing Practices: Annex 21

    Good Manufacturing Practices: Annex 21 November 16, 2022. 10:00AM EST/ 3.00PM IST Orphan Drug Consulting is hosting a series of Quality Assurance webinars for the month of November. Our first webinar will feature Sharon Cullen, Head of Quality, and Martina White, Quality Consultant from Orphan Drug Consulting. Join Sharon Cullen and Martina White as they

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  • Webinar: Key EU Regulatory Licensing Requirements

    Webinar: Key EU Regulatory Licensing Requirements

    Key EU Regulatory Licensing Requirements November 23, 2022. 10:00AM EST/ 3.00PM IST Orphan Drug Consulting is hosting a series of Quality Assurance webinars for the month of November. Our second webinar of the series will feature Kevin Lyons, Senior Quality Assurance Manager, and Sharon Cullen, Head of Quality from Orphan Drug Consulting. Join Kevin Lyons

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  • Webinar: Manufacturing Authorisation Holder Responsibilities

    Webinar: Manufacturing Authorisation Holder Responsibilities

    Manufacturing Authorisation Holder Responsibilities November 30, 2022. 10:00AM EST/ 3.00PM IST Orphan Drug Consulting is hosting a series of Quality Assurance webinars for the month of November. Our final webinar of the series will feature Martina White, Quality Consultant, and Kevin Lyons, Senior Quality Assurance Manager from Orphan Drug Consulting. Join Martina White and Kevin

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  • Orphan Drugs & Rare Diseases Global Congress 2022 Americas

    Orphan Drugs & Rare Diseases Global Congress 2022 Americas

    Join us at Orphan Drugs & Rare Diseases Global Congress 2022 Americas November 29-30, 2022. Orphan Drug Consulting is delighted to be attending the Orphan Drugs & Rare Diseases Global Congress 2022 Americas which is taking place as an event in the Hyatt Regency Boston Hotel, MA from 29th–30th November 2022. About Orphan Drugs &

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  • European Supply Strategy Workshop

    European Supply Strategy Workshop

      Join us at our Complimentary European Supply Strategy Workshop in Zurich, Switzerland. December 12, 2022.   Location: Hotel Schweizerhof Zurich, Bahnhofplatz 7 ,8001 Zurich, Switzerland Date: Monday, 12th December 2022 Workshop Time: 12:00 – 16:30 Social Event Time: 16:30 – 20:00 When preparing for a product launch in Europe, it’s important to choose the

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  • Orphan Drug Consulting Celebrates 5 Years in Business with Key Milestone Achievements in 2022

    Orphan Drug Consulting Celebrates 5 Years in Business with Key Milestone Achievements in 2022

    Dublin, Ireland, 28 September 2022 – Orphan Drug Consulting celebrates its fifth anniversary. Orphan Drug Consulting is proud to announce the celebration of 5 years in business. Since its foundation in 2017 by Evelyn Kelly, Orphan Drug Consulting has grown from a core team based in Ireland to a combined global group of 26 employees

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  • World Orphan Drug Congress Europe 2022

    World Orphan Drug Congress Europe 2022

    Join us at World Orphan Drug Congress Europe 2022 November 14-17, 2022. Orphan Drug Consulting is delighted to be exhibiting at World Orphan Drug Congress 2022 taking place as an event in the Melia Sitges Hotel, Spain from 14th–17th November 2022. Join Evelyn Kelly at World Orphan Drug Congress as she presents ‘Navigating the potential

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  • The Role of a Responsible Person (RP) & a Qualified Person (QP)

    The Role of a Responsible Person (RP) & a Qualified Person (QP)

    What is a Marketing Authorization? A marketing authorization (MA) is the authorization from the European Medicines Agency (EMA) which permits a medicine to be sold in one, several, or all the European Union’s member states, depending on the type of application that has been submitted and to which agency. What is a Qualified Person? Under

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