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Overview Live Pharmaceutical Webinars and Webinar Recordings

Next Live Webinars

 


Excipient Selection for Enhancing Bioavailability and Stability in Oral and Injectable Drug Formulations

Excipient Selection for Enhancing Bioavailability and Stability in Oral and Injectable Drug Formulations

 

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Excipient impurities causing stability failures? Formulation inconsistencies delaying your launch? Visual quality issues impacting patient confidence?

Join the webinar to discover why excipient selection from day one is critical to your formulation success and how advanced purification technologies can eliminate the hidden risks that compromise drug product quality.

Excipient quality extends beyond compendial specifications. Explore smart selection strategies for complex formulations with poorly water-soluble APIs. Prevent impurity-driven interactions that compromise stability and ensure consistent performance through commercial scale. See breakthrough purification technology achieving up to 54% reduction in color formation while maintaining full functionality.

 

Why Attend?

  • Start right: Make informed excipient choices early in development
  • Reduce risk: Prevent stability failures and batch rejections
  • Accelerate timelines: Avoid costly reformulation and launch delays
  • Build confidence: Deliver consistent, high-quality products patients trust

Perfect For:

  • Formulation scientists
  • QA/Regulatory professionals
  • R&D managers
  • CMC specialists
  • Technical decision-makers in pharma and biopharma development

What you will learn:

  • How excipient impurities can influence drug product stability, discoloration, and degradation pathways
  • Practical strategies for selecting excipients in complex formulations, especially for poorly water-soluble APIs
  • How excipient purity impacts visual consistency, stability, and manufacturability of drug products
  • How advanced purification technologies can help mitigate formulation risks

 

Date & Time & Timezone: Apr 22, 2026 04:00 PM in Amsterdam, Berlin, Rome, Stockholm, Vienna

 

Speaker:

Dr. Bhushan Thekedar
Dr. Bhushan Thekedar

Dr. Bhushan Thekedar

Head of Global Business Development, Clariant

Dr. Bhushan Thekedar is Head of Global Business Development for Healthcare at Clariant, where he leads global commercial strategy and growth initiatives for pharmaceutical excipients.

With over 15 years of experience in the life sciences industry, he has held technical and commercial leadership roles at Clariant, Merck KGaA, and BASF, focusing on formulation excipients, bioavailability enhancement technologies, and pharmaceutical ingredient solutions.

Dr. Thekedar combines a strong scientific background with global business development expertise and works closely with pharmaceutical companies to support the development of robust and high-performance drug formulations.

 

For more information & registration here:


Great science for the smallest things

Great science for the smallest things

Great science for the smallest things

 

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Gattefossé Pharmaceuticals gathers with Skyepharma and RCPE to decipher the innovative solutions for streamlining nanopharmaceutical production. During the “Great science for the smallest things” webinar, technical experts will share insights obtained during the NanoFacT consortium, in particularly:

  • The advantages of nanoparticles in drug delivery;
  • What excipients can be used to formulate nanoparticles;
  • How to scale-up nanoparticle manufacturing using continuous manufacturing;
  • A proof-of-concept with abiraterone.

 

Date & Time & Timezone: Two identical sessions are organized on March 31st 9:00 AM (CET) and on April 2nd 3:00 PM (CET).

 

Speaker:

Manon Rossano

Manon Rossano

Project Leader Pharmaceuticals at Gattefossé

Dr. Carolin Tetyczka

Dr. Carolin Tetyczka

Senior Scientist at RCPE

Vanessa Bourgeaux

Vanessa Bourgeaux

Innovation & CMC Leader at Skyepharma

Valentine Daret

Valentine Daret

PhD student at Skyepharma

 

For more information & registration here:

 


Recorded Webinars:

Nitrites Nitrosamines The impacts on analytics, but not only

Nitrites Nitrosamines The impacts on analytics, but not only

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Continuous manufacturing: Excipient characterization and formulation development Continuous manufacturing: Excipient characterization and formulation development

Continuous manufacturing: excipient characterization and formulation development

RECORDING

galenIQ™ - a new standard for binders in granulation processes

galenIQ™ – a new standard for binders in granulation processes

RECORDING

Webinar Lipid Formulations Across Generations Lifecycle Management for Adult and Pediatric Populations

Lipid Formulations Across Generations Lifecycle Management for Adult and Pediatric Populations

RECORDING

Masterclass in Nanomedicine: Olivia Merkel & Paola Luciani

Masterclass in Nanomedicine: Olivia Merkel & Paola Luciani

RECORDING

Overcoming formulation challenges: A comparative guide to selecting thickening polymers for topical drugs

Overcoming formulation challenges: A comparative guide to selecting thickening polymers for topical drugs

RECORDING

STYL’One Nano Compaction Simulator and Alix Software Demo

STYL’One Nano Compaction Simulator and Alix Software Demo

RECORDING

The Right Choice Direct Compression Lactose in Drug Development & Sustainability

The Right Choice: Direct Compression Lactose in Drug Development & Sustainability

RECORDING

Scale Up Your Scale Up – Optimizing Tablet Development for Production Success

Scale Up Your Scale Up – Optimizing Tablet Development for Production Success

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Smarter Stabilization for Lipid Nanoparticles: Formulating Biopharmaceuticals with Sucrose

Smarter Stabilization for Lipid Nanoparticles: Formulating Biopharmaceuticals with Sucrose

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The Role of Excipients in Determining Nitrosamine Risks for Drug Products

The Role of Excipients in Determining Nitrosamine Risks for Drug Products

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Optimizing Pharmaceutical Formulations: Strategies for Improving Stability and Minimizing Impurities

Optimizing Pharmaceutical Formulations: Strategies for Improving Stability and Minimizing Impurities

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Next-Gen Coatings: Merging Sustainability with Superior Performance

Next-Gen Coatings: Merging Sustainability with Superior Performance

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How to predict the impact of excipient variabilities in your tablet design

How to predict the impact of excipient variabilities in your tablet design

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Addressing topical drug formulation challenges through excipient selection

Topical drug formulation challenges

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Controlled Release for Nutraceuticals

Controlled Release for Nutraceuticals

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Rethinking the development of controlled release formulations and manufacturing processesRethinking the development of controlled release formulations and manufacturing processes

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Rational Selection of Cyclodextrins for the Solubilization of Poorly Soluble Oral Drugs

Rational Selection of Cyclodextrins for the Solubilization of Poorly Soluble Oral Drugs

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Enhanced Stability and Bioavailability of Poorly Soluble APIs

Enhanced Stability and Bioavailability of Poorly Soluble APIs

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beneo webinar - Fast Track development of Biphasic nano-dexamethasone Pellets using galenIQ™

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Webinar Roquette - Solving capping challenges using mannitolSolving capping challenges using mannitol as an excipient model

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Development of directly compressible formulations of Sitagliptin hydrochloride and Sitagliptin phosphate

Development of directly compressible formulations of Sitagliptin hydrochloride and Sitagliptin phosphate.

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Enhanced Stability and Bioavailability of Poorly Soluble APIs

Enhanced Stability and Bioavailability of Poorly Soluble APIs

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Ashland-Webinar Fast Disintegrating Tablets with Polyplasone

Formulate Robust, Fast Disintegrating Tablets with polyplasdone® crospovidone.

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Antioxidants, a safe and viable Inhibition Strategy for Nitrosamine Formation In Drug Products

Antioxidants, a safe and viable Inhibition Strategy for Nitrosamine Formation In Drug Products

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SEDDS Webinar BASFRational Selection and Application of Ready-to-Use Formulations for Self-Emulsifying Drug Delivery Systems

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Pellets from fluid bed processes – a smart concept for high(er) potent drug processing Glatt: Pellets from fluid bed processes – a smart concept for high(er) potent drug processing

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Functional Tartaric Acid Pellets in Modern Formulation Challenges
Webinar: Functional Tartaric Acid Pellets in Modern Formulation Challenges

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LIPOID_webinar_Quality Requirements for Phospholipid Excipients
Quality Requirements for Phospholipid Excipients in Liposomal Formulations

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Quality Services along the Value Chain Glatt: Quality Services along the Value Chain

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On-demand webinar: From powder to DC oral solid dosage form – galenIQ™ From powder to DC oral solid dosage form – using galenIQ™, the sweet-tasting filler binder.

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teaser image of Solving one of the biggest limitations of modern clinical trials: Patient Recruitment Solving one of the biggest limitations of modern clinical trials: Patient Recruitment

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Shin-Etsu - Downstream Processing Webinar Teaser Downstream Processing with Alexanderwerk & Shin-Etsu

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easer Shin Etsu Webinar 2 Spray Drying Spray drying with Shin-Etsu, ProCepT and Xedev

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Multiparticulates 8 Teaser Multiparticulates Part 8: Scale up considerations on the Wurster (bottomspray) fluidized bed process

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Hot-melt extrusion - on demand webinar Hot Melt Extrusion (HME) with Shin-Etsu, Leistritz and the St. John’s University

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Merck Webinar HeaderMake it Right: Best Practices for mRNA Manufacturing

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Multiparticulates 7 – Next Generation ODTS with high dosed Multiparticulates Multiparticulates 7 – Next Generation ODTS with high dosed Multiparticulates

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on demand webinar teaser of ZoomLab™: Digitally guiding dosage form and formulation for improved solubility ZoomLab™: Digitally guiding dosage form and formulation for improved solubility

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Pöllinger Webinar Multiparticulates 6 - Teaser Multiparticulates – modern oral drug products for our society; Part 6: DoE case studies in QbD development

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Merck Webinar HeaderDon’t Feed the Trolls – Crazy Powders and Electrostatic Charge in Continuous Manufacturing

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Webinar Multiparticulates 5Multiparticulates 5 – Product and process development applying QbD and DoE concepts to define DS

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Webinar Teaser galenIQ - FinalgalenIQ™ – Ask the expert!

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Addressing Raw Material Handling Challenges by Dry Granulation

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Gattefossé - Rx & OTC Product Line Extensions with Oral Lipid-Based Delivery PlatformsRx & OTC Product Line Extensions with Oral Lipid-Based Delivery Platforms

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Merck Webinar HeaderMerck: 3D Printing – shaping the future of formulation development

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Glatt webinar Multiparticulates 4b teaser

Multiparticulates 4b – Glatt Fluidbed Wurster Drug Layering and Coating – the Process

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ZoomLab™ - Interview with F BrandlZoomLab™ – The interview with Dr. Ferdinand Brandl from BASF

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webinar glatt multiparticulates basicsMultiparticulates Part IVa: Functional Coating Applications – The Basics

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On Demand Webinar Zoomlab

ZoomLab™: Digitally Predicting and Optimizing Enteric-Release Coatings Formulations

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Live Webcast Biogrund Ready-to-use FilmcoatingReady-to-Use: When Film Coating Becomes Easy, Fast & Reliable

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webcast basf catalentBASF & Catalent: Optimizing Lipid-Based Formulation For Commercial Success

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Webinar_Allison_Labriola_GlattMultiparticulates for paediatric oral drug delivery

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Webinar Ingredientpharm- Functional Starter PelletsNeutral And Functional Starter Pellets

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live webcast easy way of tableting biogrundThe Easy Way Of Tableting: Excipient Premixes For Direct Compression

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online seminar multiparticulates matrixMultiparticulates From Matric Core Pellets – Glatt CPS® Technology

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Live Webcast Biogrund Clean Label Solutions Market Trends & Clean Label Solutions for Solid Oral Dosage Forms

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live webcast qualit-e interview Qualit-E: Securely Upload And Share Quality Documents

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gattefosse webcast A beginners guide to SELF’ies for solubility and oral bioavailability enhancement

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