All NewsBio/Pharma News
All PublicationsPharmTechPharmTech Europe
MarketplaceICH Q9 Revision: A Comprehensive Resource on Quality Risk ManagementPeer-Reviewed ResearchPharmTech ProductsPharma InsightsSponsored PodcastsSponsored VideosSponsored eBooksWhitepapers
Webcasts
All VideosAsk the ExpertBehind The HeadlinesBuy, Sell, HoldDrug Digest VideosDrug Solutions PodcastPeer ExchangeSexy ScienceTech Talk
Conference CoverageConference ListingEvents
Subscribe
AnalyticsAnalyticsAnalytics
Data and Artificial Intelligence
Dosage FormsDosage FormsDosage FormsDosage FormsDosage Forms
Drug DevelopmentDrug DevelopmentDrug DevelopmentDrug DevelopmentDrug DevelopmentDrug Development
ManufacturingManufacturingManufacturingManufacturingManufacturingManufacturingManufacturingManufacturingManufacturingManufacturingManufacturingManufacturingManufacturing
OutsourcingOutsourcingOutsourcingOutsourcingOutsourcingOutsourcingOutsourcing
Quality SystemsQuality SystemsQuality SystemsQuality Systems
Spotlight -
  • Analytics
  • Dosage Forms
  • Drug Development
  • Manufacturing
  • Outsourcing
  • Quality Systems
IS1
  • Applied Clinical Trials

  • BioPharm International

  • Cannabis Science and Technology

  • Chromatography Online

  • Nutritional Outlook

  • Pharmaceutical Commerce

  • Pharmaceutical Executive

  • Pharm Tech

  • Spectroscopy Online

  • Turbo Machinery Magazine

AnalyticsAnalyticsAnalytics
Data and Artificial Intelligence
Dosage FormsDosage FormsDosage FormsDosage FormsDosage Forms
Drug DevelopmentDrug DevelopmentDrug DevelopmentDrug DevelopmentDrug DevelopmentDrug Development
ManufacturingManufacturingManufacturingManufacturingManufacturingManufacturingManufacturingManufacturingManufacturingManufacturingManufacturingManufacturingManufacturing
OutsourcingOutsourcingOutsourcingOutsourcingOutsourcingOutsourcingOutsourcing
Quality SystemsQuality SystemsQuality SystemsQuality Systems
IS1
  • Applied Clinical Trials

  • BioPharm International

  • Cannabis Science and Technology

  • Chromatography Online

  • Nutritional Outlook

  • Pharmaceutical Commerce

  • Pharmaceutical Executive

  • Pharm Tech

  • Spectroscopy Online

  • Turbo Machinery Magazine

    • Webcasts
    • Subscribe
Advertisement

Forecasting Trends in Pharma Innovation

February 15, 2023
By Ashley Wentworth
Publication
Article
Pharmaceutical TechnologyPharmaceutical Technology, Bio/Pharma Outsourcing Innovation, February 2023
Volume 2023 eBook
Issue 1

In the coming year, pharmaceutical innovation will be fueled by key trends throughout the quality sector.

TON FORIO - STOCK.ADOBE.COM

TON FORIO - STOCK.ADOBE.COM

The pace of quality transformation in life sciences continues to accelerate as global pharmaceutical companies and fast-growing biotechs look to simplify and automate complex processes. Investments in technology
are expected to continue well beyond 2023, with the quality management systems (QMS) market forecasted to grow at a 10% compound annual growth rate until 2030 (1).

Industry leaders are driving positive change and charting the path toward unified quality processes that bring together people, partners, and systems. For example, The Center for Breakthrough Medicines is a contract development and manufacturing organization (CDMO) that adopted advanced quality solutions to support its vision of building the world’s largest cell and gene therapy manufacturing and testing facility (2).

However, more work remains to stay ahead of evolving market conditions, regulatory requirements, and customer expectations. A continued commitment to driving innovation will be critical for companies to keep up with industry changes and deliver new therapeutics to patients morequickly while mitigating risks. In this article, four key trends that will shape the future of quality and manufacturing are identified, examined, and discussed.

Read this article in Pharmaceutical Technology’s February 2023 Outsourcing Innovation eBook.

Outsourcing Innovation eBook

Read the article:
Forecasting Trends in Pharma Innovation

Read the eBook:
Pharmaceutical Technology’s Outsourcing Innovation eBook

About the author

Ashley Wentworth is senior director, Vault Quality, at Veeva Systems.

Article Details

Pharmaceutical Technology
eBook: Outsourcing Innovation, February 2023
February 2023
Pages: 10–11

Citation

When referring to this article, please cite it as A. Wentworth, “Forecasting Trends in Pharma Innovation" Pharmaceutical Technology Outsourcing Innovation eBook (February 2023).

Articles in this issue

BillionPhotos.com/Stock.adobe.com – preparing for emerging mRNA technologies requires adapting fill/finish and cold chain capabilities.
Preparing for a New Wave of mRNA Technologies
CRO advances
CROs Gaining a Competitive Edge
Biopharmaceutical Manufacturing Growth
Biopharmaceutical Manufacturing Growth
Forecasting Trends in Pharma Innovation
Forecasting Trends in Pharma Innovation
information transfer
Communication is Key in Complex Tech Transfer
Scaling Manufacturing Processes Using Single-Use Technologies
Scaling Manufacturing Processes Using Single-Use Technologies
Recent Videos
Behind the Headlines, Episode 18
Behind the Headlines, Episode 18: Sanofi, GSK Go Big in M&A, mRNA Momentum Falters, and More
A CDMO’s Role in API Quality
A CDMO’s Role in API Quality
CPHI Americas 2025: The Evolving Role of the CDMO
CPHI Americas 2025: The Evolving Role of the CDMO
Drug Digest: Patient Preference Drives Solid Dosage Trends
Drug Digest: Patient Preference Drives Solid Dosage Trends
Ask the Expert: Quality Control Units
Ask the Expert: Quality Control Units
Behind the Headlines, Episode 17
Behind the Headlines, Episode 17: Bespoke CRISPR Therapy, Executive Order Fallout, and More
AAPS National Biotechnology Conference 2025: High-Concentration Biologics
AAPS National Biotechnology Conference 2025: High-Concentration Biologics
Industry Outlook 2025: The Future of Technology in the Biopharma Industry
Industry Outlook 2025: The Future of Technology in the Biopharma Industry
AAPS National Biotechnology Conference 2025: AAV Vector Production
AAPS National Biotechnology Conference 2025: AAV Vector Production
Industry Outlook 2025: European Geopolitical Impact on Pharma
Industry Outlook 2025: European Geopolitical Impact on Pharma
Related Content
Advertisement

Three groups of people are connected by lines. Coordination and knowledge sharing. Outsourcing. | Image Credit: © Uladzislau - stock.adobe.com

Market Demands and Emerging Technologies Shape Outsourcing Models

Patrick Lavery
June 5th 2025
Article

Trends in certain forms of drug delivery, as well as the emergence of artificial intelligence, are playing roles in evolving the nature of partnerships, but there are new types of partnerships gaining steam as well.


Drug Solutions Podcast: Growth and Advancements in Fill/Finish

Drug Solutions Podcast: Growth and Advancements in Fill/Finish

Felicity Thomas
June 25th 2024
Podcast

In this episode, Hanns-Christian Mahler from ten23 Health chats about the advances in fill/finish.


Landkarte *** Europa | Image credit: ©beugdesign - Stock.adobe.com

EMA Is Tackling Vulnerabilities in the Supply Chain of Radiopharmaceuticals

Cheryl Barton
June 4th 2025
Article

EMA has published recommendations to address potential radiopharmaceutical shortages.


Drug Solutions Podcast: All About Data: Looking at the EHDS in More Detail

Drug Solutions Podcast: All About Data: Looking at the EHDS in More Detail

Felicity Thomas
May 28th 2024
Podcast

In this episode, Alexander Natz from EUCOPE chats about the European Health Data Space.


Question mark background | Image Credit: © Leigh-Prather - © Leigh Prather - stock.adobe.com

Guidance on Quality Culture Standards

Matt Cushing;Susan J. Schniepp
June 3rd 2025
Article

Matt Cushing, VP of Quality and Science, Nelson Labs, and Susan J. Schniepp, distinguished fellow at Regulatory Compliance Associates, a Nelson Labs Company, discuss PDA/ANSI Standard 06-2025: Assessment of Quality Culture Guidance Documents, Models, and Tools, which was published in February 2025.


inscription on the courthouse | Image Credit: © bluraz - stock.adobe.com

Eisai Wins Judgment Against Shilpa Over Sale of Lenvatinib Mesylate Generic

Patrick Lavery
June 2nd 2025
Article

As a result of the decision, Shilpa will not be eligible to receive FDA approval for its lenvatinib mesylate generic until February 2036.

Related Content
Quality Systems
|
Outsourcing
|
Bio/Pharma Business
|
Contract Development Services
|
Drug Development
Advertisement

Three groups of people are connected by lines. Coordination and knowledge sharing. Outsourcing. | Image Credit: © Uladzislau - stock.adobe.com

Market Demands and Emerging Technologies Shape Outsourcing Models

Patrick Lavery
June 5th 2025
Article

Trends in certain forms of drug delivery, as well as the emergence of artificial intelligence, are playing roles in evolving the nature of partnerships, but there are new types of partnerships gaining steam as well.


Drug Solutions Podcast: Growth and Advancements in Fill/Finish

Drug Solutions Podcast: Growth and Advancements in Fill/Finish

Felicity Thomas
June 25th 2024
Podcast

In this episode, Hanns-Christian Mahler from ten23 Health chats about the advances in fill/finish.


Landkarte *** Europa | Image credit: ©beugdesign - Stock.adobe.com

EMA Is Tackling Vulnerabilities in the Supply Chain of Radiopharmaceuticals

Cheryl Barton
June 4th 2025
Article

EMA has published recommendations to address potential radiopharmaceutical shortages.


Drug Solutions Podcast: All About Data: Looking at the EHDS in More Detail

Drug Solutions Podcast: All About Data: Looking at the EHDS in More Detail

Felicity Thomas
May 28th 2024
Podcast

In this episode, Alexander Natz from EUCOPE chats about the European Health Data Space.


Question mark background | Image Credit: © Leigh-Prather - © Leigh Prather - stock.adobe.com

Guidance on Quality Culture Standards

Matt Cushing;Susan J. Schniepp
June 3rd 2025
Article

Matt Cushing, VP of Quality and Science, Nelson Labs, and Susan J. Schniepp, distinguished fellow at Regulatory Compliance Associates, a Nelson Labs Company, discuss PDA/ANSI Standard 06-2025: Assessment of Quality Culture Guidance Documents, Models, and Tools, which was published in February 2025.


inscription on the courthouse | Image Credit: © bluraz - stock.adobe.com

Eisai Wins Judgment Against Shilpa Over Sale of Lenvatinib Mesylate Generic

Patrick Lavery
June 2nd 2025
Article

As a result of the decision, Shilpa will not be eligible to receive FDA approval for its lenvatinib mesylate generic until February 2036.

Advertisement
Advertisement
Advertisement
x
About Us
Advertise
Contact Us
Editorial Info
Editorial Advisory Board
Do Not Sell My Personal Information
Privacy Policy
Terms and Conditions
Contact Info

2 Commerce Drive
Cranbury, NJ 08512

609-716-7777

© 2025 MJH Life Sciences

All rights reserved.