White paperThe Enterprise Framework for Compliant, Scalable AI
Download now

2022 Trends in Life Sciences

Download USDM's 2022 life sciences trends white paper for guidance on data analytics, Computer Software Assurance, GxP process automation, strategic partnerships, and employee experience in regulated organizations.

2022 Trends in Life Sciences
White Paper

Download this white paper

Download USDM's 2022 life sciences trends white paper for guidance on data analytics, Computer Software Assurance, GxP process automation, strategic partnerships, and employee experience in regulated organizations.

Fill out the short form to access the requested download.

We only use your details to deliver this download and follow up on your request. No newsletter detour. Unsubscribe anytime.

Agree to Privacy Policy and Email Opt-In *

By submitting this form, you agree to USDM’s Privacy Policy and consent to receive communications from USDM. You can unsubscribe at any time using the link in our emails.

Modern life sciences teams need faster insight, stronger control, and better ways to execute regulated work.

The 2022 Trends in Life Sciences white paper looks at the operational shifts that continue to shape pharma, biotech, and medical device organizations: decision intelligence, Computer Software Assurance, AI-enabled process automation, ecosystem collaboration, and employee experience.

The original trends were written for 2022, but the operating questions are still current. How do regulated companies turn data into decisions? How do they reduce validation drag without weakening evidence? How do they automate GxP processes responsibly? And how do they give employees tools that make controlled work easier instead of more manual?

What you will learn

  • Prepare for decision intelligence: connect GxP and non-GxP data into usable models that support faster, better-controlled decisions.
  • Reduce validation friction: understand why Computer Software Assurance and risk-based testing matter for modern regulated technology programs.
  • Automate with control: evaluate where AI-infused GxP process automation can improve efficiency, visibility, and compliance evidence.
  • Govern partner ecosystems: plan for collaboration across technology providers, consultants, regulators, and nontraditional industry participants.
  • Improve the employee experience: design technology and workflows that help teams do their best work without adding avoidable administrative drag.

Why these trends still matter

Life sciences organizations have become more data-rich, platform-dependent, and partner-driven. That creates opportunity, but it also increases the need for governance. Data analytics, cloud platforms, process automation, and AI-enabled capabilities only create value when they are tied to clear ownership, reliable evidence, and inspection-ready operating models.

This white paper is useful for teams that want a concise view of the forces changing regulated operations and the practical questions leaders should ask before modernizing systems, workflows, and quality processes.

USDM point of view Transformation in life sciences is not a technology shopping exercise. It is an operating-model discipline: define the process, control the data, validate what matters, and keep evidence available when regulators or customers ask hard questions.

KPIs to track modernization readiness

Use these program metrics to turn the white paper themes into a practical internal review. These are measurement categories to track, not invented performance claims.

Program metrics to track
Data readinessDecision-data availabilityPriority business decisions supported by current, governed, accessible GxP and non-GxP data sources.
ValidationRisk-based test focusCritical requirements with traceable evidence divided by total requirements requiring validation attention.
AutomationManual workflow burdenRecurring process steps still handled by email, spreadsheets, duplicate entry, or uncontrolled handoffs.
AdoptionEmployee experience frictionValidated systems and processes reviewed for training effort, usability issues, rework, and avoidable support demand.

What the white paper covers

  • Decision intelligence and data analytics: why companies need better data integration, scalable architecture, and access to the right operational signals.
  • Computer Software Assurance: how CSA and automation can simplify validation while keeping evidence focused on risk and intended use.
  • GxP process automation: where AI-infused capabilities can help regulated teams improve efficiency, insight, and process visibility.
  • Collaboration for the greater good: why life sciences innovation increasingly depends on partnerships across technology, healthcare, regulatory, and operating teams.
  • Employee experience: how better systems and workflows help teams execute regulated work with less friction.

Who should download it

  • Quality, validation, and IT leaders modernizing regulated systems and validation practices.
  • Digital transformation leaders evaluating automation, analytics, and AI-enabled workflows.
  • Compliance and operations teams trying to reduce manual work while keeping inspection evidence strong.
  • Executives planning life sciences technology strategy across platforms, partners, and internal teams.
Related next step If your team is modernizing regulated workflows, USDM can help assess your current operating model, prioritize risks, and build a roadmap for controlled automation, CSA, data governance, and continuous compliance. Talk to USDM about modernization readiness.

Download the white paper

Fill out the short form above to access the complete download.

Explore capabilities

Find the USDM practice area most relevant to this topic.

Platform partners

See how USDM delivers outcomes on the platforms you use.

Related resources

Keep exploring

Hand-picked blogs, case studies, and guides on the same topic.

AI deploymentGovernance

Automating Software License Procurement in ServiceNow

Mid-sized life sciences therapeutics company managing software asset licenses and entitlements across vendors in ServiceNow.

Discover how USDM automated software license procurement for a life sciences company, reducing errors, improving compliance, and increasing ROI by 30%.

ROI Increase

30%

See proof
GovernanceContinuous compliance

Optimized Use of TraceLink Helps Pharma Company Implement Serialization

Specialty pharmaceutical company focused on autoimmune disease therapies, with no prior serialization experience and no in-house TraceLink expertise.

Case study on Optimized Use of TraceLink Helps Pharma Company Implement Serialization.

Delivery

On Time, Under Budget

See proof
White Paper

Google Cloud Platform for Life Sciences and Health Technology

A white paper on building secure, inspection-ready Google Cloud programs for life sciences — aligning GxP controls, identity and access, data governance, DevOps evidence, and USDM Cloud Assurance from the start.

Read
White Paper

Regulated GxP Workloads in the Public Cloud

A USDM white paper on running regulated GxP workloads in the public cloud — why life sciences lagged on cloud adoption, what changed, and how continuous compliance with USDM Cloud Assurance spans IaaS, PaaS, and SaaS.

Read
AI deploymentGovernance

CMDB Remediation for a Mid-Sized Therapeutics Company

Mid-sized life sciences therapeutics company that recently relocated and had no in-house ServiceNow developers.

Discover how USDM improved IT compliance and efficiency for a therapeutics company by optimizing CMDB, automating discovery, and reducing data errors by 25%.

ROI improvement

30%

See proof
GovernanceContinuous compliance

Complaint Handling Integration with Salesforce Improves Patient Care

An FDA-cleared medical device company with a patient-based app, patented micro-sensor and Bluetooth technology designed to deliver value-based care and reinforce adherence to treatment.

Case study on Complaint Handling Integration with Salesforce Improves Patient Care.

Time to qualification

3 months

See proof