Webinar Services for Pharma, Biotech, Medtech

Expert-led webinars that connect life sciences leaders with the insights, solutions and partners they need to move their work forward.

42%

Average engagement rate

Across webinars

Upcoming Webinars

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9

Dec

15:00 (GMT) / 10:00 (EST)

Developing Nasal Drug Delivery's Next Generation: Psychedelics and CNS

How formulation and manufacturing strategies are evolving to support nasal drug delivery's expansion beyond traditional local and systemic therapies

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09/12/2026

19

Nov

16:00 CET - 10:00 ET

HUGO-Nano: The Next Generation of Fully Human VHH Antibodies

HUGO-Nano mouse generates fully human, developable single-domain antibodies (VHHs) with no post-discovery humanization required.

Register Now

19/11/2026

3

Dec

4pm (CET) / 10am (ET)

Advancing Autoinjector Platforms for Evolving Drug and Patient Needs

How adaptable platform technology can address diverse drug profiles, patient needs and brand requirements without starting device development from scratch.

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03/12/2026

17

Sep

16:00 CEST - 10:00 ET

Feasibility to Phase I: How Early Development Decisions Save Time and Cost

Discover how to assess API suitability for oral films and transdermal patches, reduce time and cost, and optimise formulations

Register Now

17/09/2026

9

Jul

16:00 CEST - 10:00 ET

Characterize Your Biologics with Smart and Science-driven Concepts

How to choose the best panel of phase-appropriate analytical methods for complex modalities while maintaining aggressive development timelines

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09/07/2026

23

Jul

15:00 (BST) / 10:00 (EDT)

Sterile Drug Products: Phase I Development in a Post-Annex 1 Environment

Annex 1 has raised the bar for sterile drug product development. A structured single-site approach could be the fastest route to Phase I.

Register Now

23/07/2026

24

Sep

4pm (CET) / 10am (ET)

Hypodermic Needle
Secure your Value Proposition
by Co-Packing

Needle choice is rarely a headline decision, yet it contributes to the treatment experience and efficacy.

Register Now

24/09/2026

1

Dec

16:00 CET - 10:00 ET

Stability by design: Connecting formulation science and primary packaging strategy

Learn how early formulation and primary packaging integration reduces risk for high-concentration, large-volume biologics.

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01/12/2026

3pm (GMT) / 10am (ET)

Packaging Precision: Insights on Ensuring Stability and Shelf-Life

Capsule and packaging material selection for OSD formulations, strategies for overcoming stability challenges and cost optimisation during scale up.

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07/03/2024

11am (ET) / 10am (ET)

Master the Next Generation of Clinical Research: 5 Strategies to Dramatically Improve Data Quality

Five strategies for clinical data quality, covering data management, risk based quality management, AI assisted review and proactive error detection.

Medidata blue logo

Register Now

08/05/2024

4pm (CET) / 10am (ET)

Preservative-Free Spray Applications and Their Compliant Road to Market

Preservative-free spray system options, drug device combination under EU MDR and regulatory documentation requirements for market entry.

Register Now

27/06/2024

4pm (CET) / 10am (ET)

Innovative Solutions in Pre-Filled Syringes for Biologics and Ophthalmic Applications

Selecting the right pre-filled syringe for biologics and ophthalmic applications, covering plasma coating, viscosity, compatibility and analytics.

Register Now

11/07/2024

4pm (CET) / 10am (ET)

Sharpening the Future: New Opportunities for Implant Injection

Drug implant technology advances, applicator design, manufacturing quality standards and market opportunities for long acting implant systems.

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01/10/2024

4pm (CET) / 10am (ET)

Unlocking Success in Inhaled & Nasal Drug Clinical Studies

Critical factors in OINDP clinical development, CMC risk mitigation and how to balance preparation levels to meet regulatory expectations.

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22/10/2024

4pm (CET) / 10am (ET)

How RTU Solutions Can Meet GMP Annex 1 Requirements

Pre-sterilised ready to use containers as a compliant aseptic solution, reducing contamination risk and simplifying EU GMP Annex 1 compliance.

Register Now

14/11/2024

3pm (GMT) / 10am (ET)

Transitioning an Oral Solid Dosage from Phase 1 to Phase 2 studies: Formulation challenges and strategies

Development timelines, formulation optimisation strategies and CDMO selection for transitioning oral solid dosage forms from Phase 1 to Phase 2.

Register Now

26/02/2025

4pm (CET) / 10am (ET)

EU GMP Annex 1: New Standards for Injectable Drug Manufacturing

Revised EMA GMP Annex 1 guidelines, impact on contamination control strategy and the role of primary packaging suppliers in sterility assurance.

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08/04/2025

4pm (CET) / 10am (ET)

Advancements in On-Body Drug Delivery Systems: Overcoming Challenges and Driving Innovation

Advances in on-body delivery for high volume and viscous drugs, with strategies for optimising platforms from prototype through to clinical readiness.

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10/04/2025

16:00pm (CET) / 10am (ET)

Overcoming Challenges in Preclinical Studies for Intranasal and Inhalation Programs

Preclinical intranasal and inhalation protocols, covering system selection, animal model design, insufflator and micro sprayer technologies.

Register Now

29/05/2025

16:00pm (CEST) / 10am (EDT)

Unlocking the Future of Drug Development: How PBBM & Solid Form Screening Drive Early-Phase Success

Solid form screening, PBBM modelling and in vitro testing to identify absorption risks, guide form selection and accelerate early phase development.

Register Now

05/06/2025

15:00pm (BST) / 10:00am (ET)

Navigating the sterile fill finish CDMO landscape for development and manufacturing success

CDMO capability assessment, facility design, EU GMP Annex 1 compliance and formulation strategies for sterile liquid and powder drug products.

Register Now

25/06/2025

4pm (CET) / 10:00am (ET)

Targeting the Airways: Innovations in Soft Mist Drug Delivery for All Ages – Including Infants

Soft mist aerosol technology for targeted respiratory deposition across all age groups, including a pacifier-based delivery interface designed for infants.

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09/07/2025

16:00 (CET) / 10am (ET)

Could Transmucosal Delivery Be the Right Route for Your API?

API requirements for transmucosal delivery, Mucofilm compatibility and key development steps from feasibility through to commercial manufacture.

Register Now

10/09/2025

17:00 (CET) / 11:00 (EST)

Managing the uncertainty in treatment exposure to increase success in clinical trials

Digital adherence monitoring, RBQM integration and the estimand framework to reduce trial variability and strengthen exposure response analysis.

Register Now

16/09/2025

4pm (CET) / 10am (ET)

Holistic approach to Intravitreal Injection combining Packaging and Device

The full value chain for intravitreal injection, from primary packaging and coating technology to filtered needle selection and USP 789 particle compliance.

Register Now

18/09/2025

15:00 (BST) / 10:00 (ET)

Nose-to-Brain Drug Delivery and Device Selection

Key delivery targets, transport mechanisms and device considerations for nose to brain CNS delivery, from formulation to regulatory submission.

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01/10/2025

16:00 CET / 10:00 ET

Unlocking Therapeutic Potential Through Nasal Drug Repositioning

Evaluating nasal repositioning potential, covering clinical suitability, regulatory strategy, delivery system selection and commercial impact.

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13/11/2025

15:00 (GMT) / 10:00 (ET)

Scaling Up Oral Solid Dose Manufacturing for Late-Phase Success

How to select the right CDMO, translate lab data into scalable OSD processes and apply QbD principles to avoid delays in late-phase manufacturing.

Register Now

25/03/2026

24

Nov

4pm (CET) / 10am (ET)

Moving circularity forward in medical device packaging

Learn how Tyvek® with Renewable Attribution is helping accelerate circularity in medical device packaging.

Register Now

24/11/2026

4pm (CET) / 10am (ET)

Developability Assessment and Early Formulation Studies for Biologics

Candidate selection, biophysical characterisation and pre-formulation screening to reduce late stage failures and build a strong data foundation.

Register Now

27/02/2025

4pm (CET) / 10am (ET)

Paving the way to a successful AAV product

Analytical methods for AAV characterisation, quality attributes for manufacturing and orthogonal approaches for infectivity and capsid ratios.

Register Now

20/11/2024

4pm (CET) / 10am (ET)

Lyo-Modelling Reduce risks on the road to commercialization through process understanding

Lyophilisation modelling for primary drying optimisation, robustness analysis and in silico assessment of process failures to ensure product quality.

Register Now

10/07/2024

4pm (CET) / 10am (ET)

Shedding light on surfactants used as excipient for biologics

Polysorbate degradation mechanisms, surfactant characterisation strategies and multidimensional chromatography for surfactant analysis in biologics.

Register Now

07/05/2024

4pm (CET) / 10am (ET)

Road To Success: Mapping drug development from preclinical to commercialization

A phase appropriate development roadmap for biologics, covering formulation, analytical characterisation and derisking from preclinical to market.

Register Now

21/02/2024

4pm (CET) / 10am (ET)

Every particle matters

Particle identification and characterisation tools for biologics and cell and gene therapy, covering origins, analytical methods and troubleshooting.

Register Now

29/11/2023

16:00pm (CET) / 10:00am (ET)

Smarter Drug Development for Biologics with In Silico Modelling

Computational approaches to biologics developability, formulation optimisation and stability prediction, with case studies on risk reduction.

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01/07/2025

16:00pm (CET) / 10:00am (ET)

Subvisible Particle Analysis: Ensuring Quality from Lab Bench to GMP

Regulatory requirements, method validation and variability control for subvisible particle analysis from R&D through to GMP compliance.

Register Now

18/11/2025

5

Mar

16:00pm (CET) / 10:00am (ET)

Formulating the Future:
Nucleic Acid Therapeutics Explained

Critical quality attributes for mRNA-LNP formulations, LNP delivery system stability and the analytical toolbox for nucleic acid therapeutics.

Register Now

05/03/2026

25

June

16:00pm (CEST) / 10am (EDT)

Simplifying ADC Development: An Integrated Path from Concept to Commercialization

Best practices for scalable ADC manufacturing, end to end integration and reducing complexity across the full ADC development lifecycle.

Register Now

25/06/2026

On Demand Webinar Library

Biotech

30

Stability by design: Connecting formulation science and primary packaging strategy

Watch Now

01/12/2026

Medtech

30 min

Advancing Autoinjector Platforms for Evolving Drug and Patient Needs

Watch Now

03/12/2026

Pharma

30 min

Developing Nasal Drug Delivery’s Next Generation: Psychedelics and CNS

Watch Now

09/12/2026

Biotech

30 min

HUGO-Nano: The Next Generation of Fully Human VHH Antibodies

Watch Now

19/11/2026

Medtech

30 min

Moving circularity forward in medical device packaging

Watch Now

24/11/2026

Pharma

67 min

Hypodermic Needle – Secure your Value Proposition by Co-Packing

Watch Now

24/09/2026

Pharma

47 min

Feasibility to Phase I: How Early Development Decisions Save Time and Cost

Watch Now

17/09/2026

Biotech

42 min

Sterile Drug Products: Phase I Development in a Post-Annex 1 Environment

Watch Now

23/07/2026

Biotech

57 min

Characterize Your Biologics with Smart and Science-driven Concepts

Watch Now

09/07/2026

Biotech

30 min

Simplifying ADC Development: An Integrated Path from Concept to Commercialization

Watch Now

25/06/2026

Biotech

30 min

Formulating the Future: Nucleic Acid Therapeutics Explained

Watch Now

05/03/2026

Pharma

30 min

Scaling Up Oral Solid Dose Manufacturing for Late-Phase Success

Watch Now

25/03/2026

Biotech

30 min

Subvisible Particle Analysis: Ensuring Quality from Lab Bench to GMP

Watch Now

18/11/2025

Pharma

30 min

Unlocking Therapeutic Potential Through Nasal Drug Repositioning

Watch Now

13/11/2025

Pharma

30 min

Nose-to-Brain Drug Delivery and Device Selection

Watch Now

01/10/2025

Pharma

30 min

Managing the uncertainty in treatment exposure to increase success in clinical trials

Watch Now

16/09/2025

Pharma

30 min

Could Transmucosal Delivery Be the Right Route for Your API?

Watch Now

10/09/2025

Medtech

30 min

Holistic approach to Intravitreal Injection combining Packaging and Device

Watch Now

18/09/2025

Biotech

30 min

Smarter Drug Development for Biologics with In Silico Modelling

Watch Now

01/07/2025

Medtech

30 min

Targeting the Airways: Innovations in Soft Mist Drug Delivery for All Ages – Including Infants

Watch Now

09/07/2025

Pharma

30 min

Navigating the sterile fill finish CDMO landscape for development and manufacturing success

Watch Now

25/06/2025

Pharma

30 min

Overcoming Challenges in Preclinical Studies for Intranasal and Inhalation Programs

Watch Now

29/05/2025

Pharma

30 min

Unlocking the Future of Drug Development: How PBBM & Solid Form Screening Drive Early-Phase Success

Watch Now

05/06/2025

Pharma

30 min

EU GMP Annex 1: New Standards for Injectable Drug Manufacturing

Watch Now

08/04/2025

Biotech

30 min

Every particle matters

Watch Now

29/11/2023

Biotech

30 min

Road To Success: Mapping drug development from preclinical to commercialization

Watch Now

21/02/2024

Pharma

30 min

Packaging Precision:Insights on Ensuring Stability and Shelf-Life

Watch Now

07/03/2024

Medidata webinar upcoming
Pharma

30 min

Master the Next Generation of Clinical Research:5 Strategies to Dramatically Improve Data Quality

Medidata White logo

Watch Now

08/05/2024

Coriolis_Webinar_Surfactant_Landingpage
Biotech

30 min

Shedding light on surfactants used as excipient for biologics

Watch Now

07/05/2024

Medtech

30 min

Advancements in On-Body Drug Delivery Systems: Overcoming Challenges and Driving Innovation

Watch Now

10/04/2025

Medtech

30 min

Preservative-Free Spray Applications and Their Compliant Road to Market

Watch Now

27/06/2024

Medtech

30 min

Innovative Solutions in Pre-Filled Syringes for Biologics and Ophthalmic Applications

Watch Now

11/07/2024

Biotech

30 min

Lyo-ModellingReduce risks on the road to commercialization through process understanding

Watch Now

10/07/2024

Gaplast-Homepage
Medtech

30 min

Sharpening the Future: New Opportunities for Implant Injection

Watch Now

01/10/2024

Biotech

30 min

Paving the way to a successful AAV product

Watch Now

20/11/2024

Pharma

30 min

Unlocking Success in Inhaled & Nasal Drug Clinical Studies

Watch Now

22/10/2024

Stevanato Webinar Landing page
Pharma

30 min

How RTU Solutions Can MeetGMP Annex 1 Requirements

Watch Now

14/11/2024

Biotech

30 min

Developability Assessment and Early Formulation Studies for Biologics

Watch Now

27/02/2025

Pharma

30 min

Transitioning an Oral Solid Dosage from Phase 1 to Phase 2 studies: Formulation challenges and strategies

Watch Now

26/02/2025

Webinar Services for
Pharma, Biotech, Medtech

Pharma webinar services that reach the right audience. We run webinar campaigns for pharma, biotech and medtech organisations, from audience targeting and promotion through to live delivery and follow up. Our webinars average a 42% engagement rate.

Starting with the right audience

Every programme starts with one question: who needs to hear this? Our webinar services for pharma begin with the people who register, so they are the decision makers your objectives depend on. Before we plan a session, we agree the audience, the job role and the decision each attendee is likely to make. That shapes the speaker, the promotion and the follow up.

Each campaign is then shaped around the problem your audience is trying to solve, whether that is formulation, clinical development, regulatory readiness or manufacturing. A session for formulation scientists needs different language and evidence from one for clinical leads, so we tailor the programme to match.

Our webinar services for pharma, biotech and medtech cover the full value chain, from early development and formulation through to CDMO selection, sterile manufacturing and scale up. Pharma sessions often focus on manufacturing, Annex 1 compliance and the choice of CDMO, while also covering regulatory expectations for each stage.

Biotech sessions cover biologics characterisation, developability and analytics for antibodies, ADCs and gene therapies. These topics need early data and clear decisions, so the sessions are built to help teams choose methods, assess risk and move forward with confidence.

Medtech sessions focus on the devices and packaging that deliver those products, from autoinjectors and prefilled syringes to needles and packaging compliance. Device and packaging decisions affect usability, supply and regulatory submissions, so we cover how those choices connect to the drug itself.

Our webinar services for pharma handle the whole session, from live presentation management and speaker coordination to Q&A, polls, technical support and recording capture. Our team manages the technical side from the first rehearsal to the final recording, so your speakers can focus on the content.Sessions run cleanly from start to finish, and any issues on the day are resolved in real time. Attendees get a smooth experience, and you get a recording you can use after the event.

Within our webinar services for pharma, audience engagement starts before the webinar, with targeted email and LinkedIn outreach that builds interest in advance. During the session, attendees take part through live Q&A and polls, which shows what the audience cares about. After the event, we send personalised outreach and nurture sequences, so that interest turns into conversations.Within our webinar services for pharma, audience engagement starts before the webinar.

Ready to plan your next programme? Tell us your therapeutic area, target audience and timeline, and we will suggest a format, speaker profile and schedule. For wider reach, our executive events bring senior leaders together in invite-only settings, and Industry Intelligence gives your audience context beyond a single session. For background on the regulations many of our sessions cover, the EU GMP guidelines are a useful starting point.

Webinar services for pharma audience targeting

Right Audience

We connect you with engaged life sciences professionals across Pharma, biotech and medtech.

Expert-Led Content

High-quality, independent content developed with industry experts and trusted by your peers.

Proven Engagement

Our webinars deliver exceptional engagement, with an average engagement rate of 42%.

End to-End Support

From strategy and promotion to delivery and follow-up, we handle every detail.

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Your Experience?

Expert-led webinars that connect life sciences leaders with the insights, solutions and partners they need to move their work forward.