Digital Nova Scotia

Practical Utilization of AI for Life Sciences

AI is transforming how pharmaceutical, biotech, and MedTech organizations operate, and this microcredential gives life sciences professionals the practical, hands-on skills to lead that change. Designed specifically for non-technical roles in R&D, Regulatory Affairs, Clinical Operations, and Commercial teams, the program makes AI accessible, relevant and immediately applicable to your day-to-day work.

You’ll explore what AI is and how it fits into drug development, regulatory strategy, and operational workflows—while understanding the compliance, privacy, and quality standards that govern the industry. Through guided, applied learning, you’ll discover how to automate manual data processes, accelerate research cycles, and support regulatory submissions without compromising GxP or data protection requirements.

Course length
Date
Format
Price
6 weeks | 12 to 14 hours per week
April 27 – June 8, 2026
Virtual, online course with mandatory live sessions
$189 + HST (DNS Members) | $736 +HST (Non-DNS Members)
Course length
Date
Format
Price
6 weeks | 12 to 14 hours per week
April 27 – June 8, 2026
Virtual, online course with mandatory live sessions
$189 + HST (DNS Members) | $736 +HST (Non-DNS Members)

*Full price for this course is $739 +HST, but with support from the Atlantic Canada Opportunities Agency, Nova Scotian’s are eligible for this discounted price. Please fill in the form below.

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This program is delivered in partnership with Life Sciences Nova Scotia, and St. Francis Xavier, supporting the growth and advancement of Nova Scotia’s life sciences ecosystem.

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Practical Utilization of AI for Life Sciences

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About this course

Course overview

  • Applied AI for Pharma & Biotech Operations: Develop practical skills in using AI tools such as Perplexity AI, Notion AI, AskReg, and Cohere to streamline research, regulatory, and clinical workflows.
  • Workflow automation & knowledge management: Learn to synthesize scientific literature, clinical documentation, and regulatory guidance into searchable knowledge bases while automating repetitive documentation tasks.
  • Regulatory & Compliance Readiness (North America focus): Apply AI within FDA and Health Canada frameworks while aligning with GxP standards, HIPAA, and PIPEDA privacy requirements.
  • Practical Implementation & Capstone Project: Design and validate a custom “Multi-Tool Chain” workflow that saves a minimum of five hours of manual work per week.

Modules

  • Module 1: Foundations and AI Opportunities in Life Sciences
    • Differentiate between various Large Language Model (LLM) architectures and understand their strengths in research, logic, and data retrieval.
    • Identify high-ROI opportunities for AI implementation across drug discovery, regulatory, and clinical operations.
    • Analyze departmental workflows to pinpoint manual data silos suitable for automation.
    • Use Perplexity AI for scientific research and literature mapping.
    • Hands-on assignment: Select a recurring manual task in your department (e.g., literature monitoring or competitive intelligence). Develop a one-page “Opportunity Map” outlining current steps, AI intervention points, and expected efficiency gains.
  • Module 2: GenAI for Documentation, Data & Knowledge Systems
    • Synthesize unstructured technical data (e.g., PDFs, clinical transcripts) into centralized, searchable knowledge bases using Notion AI.
    • Develop AI-assisted workflows for drafting SOPs, research summaries, and operational documents.
    • Implement verification and self-correction strategies to mitigate hallucinations and maintain data integrity.
    • Explore enterprise data search concepts using Cohere.
    • Hands-on assignment: Design a “Living SOP” workflow using a knowledge-base approach. Identify three complex cross-document questions that extract actionable operational or clinical insights.
  • Module 3: AI Safety, Privacy & Regulatory Intelligence
    • Navigate FDA (U.S.) and Health Canada regulatory requirements using AI-augmented tools such as AskReg.
    • Evaluate AI deployment models (private vs. public environments) against HIPAA and PIPEDA privacy standards.
    • Establish audit trails for AI-generated outputs to maintain GxP compliance.
    • Identify ethical risks, including bias in clinical trial design and regulatory reporting.
    • Hands-on assignment: Conduct a compliance gap analysis comparing a U.S. and Canadian regulatory requirement. Develop a documented “Prompt Audit Trail” demonstrating traceability for regulatory review.
  • Module 4: Practical GenAI Utilization & Capstone
    • Architect multi-stage AI workflows linking research, drafting, and compliance validation.
    • Design specialized AI agents tailored to organizational regulatory history and documentation standards.
    • Quantify operational efficiency gains through structured workflow analysis.
    • Integrate multiple AI tools into a seamless operational pipeline.
    • Capstone Project: Design a “Multi-Tool Chain” workflow for a project such as a Clinical Study Report or New Drug Submission. Demonstrate how the workflow saves at least five hours of manual labor per week. Capstone submissions are presented as a video presentation.

Course schedule

Live sessions are mandatory; however, if you require an exception, please speak with the facilitator

  • Week 1 | Participant Onboarding
    • Start Date: Monday, March 23 2026 | Onboarding
  • Week 2 | Module 1: Foundations and AI Opportunities
    • Start Date: Saturday, March 28, 2026 | Asynchronous learning
    • Virtual Live session: Saturday, April 4, 2026 | 9:30AM – 12:30PM
  • Week 3 | Module 2: GenAI for Documentation and Data
    • Start Date: Monday, April 6, 2026 | Asynchronous learning
    • Virtual Live session: Saturday, April 11, 2026 | 9:30AM – 12:30PM
  • Week 4 | Module 3: AI Safety and Regulations
    • Start Date: Monday, April 13, 2026 | Asynchronous learning
    • Virtual Live session: Saturday, April 18, 2026 | 9:30AM – 12:30PM
  • Week 5 | Module 4: Practical GenAI Utilization
    • Start Date: Monday, April 20, 2026 | Asynchronous learning
    • Virtual Live session & Capstone Introduction: Saturday, April 25, 2026 | 9:30AM – 12:30PM
  • Week 6 | Capstone Project Q&A
    • Virtual Live Session: Saturday, May 2, 2026 | 9:30AM - 10:30 AM
  • Week 7 | Capstone Project Submission
    • Sunday, May 10, 2026 | Submit video presentation

Course requirements

This program utilizes a combination of AI tools and practical workflow exercises. Some tools may require short-term trials or managed demo environments.

  • Other software and hardware required:
    • Google account
    • Internet access
    • Laptop or desktop device (macOS or Windows)
    • Perplexity AI (Pro access recommended)
    • Notion AI
    • AskReg
    • Cohere (managed instance/demo access)

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Your Instructors

Instructor 1

About the instructor

Dr. Pawan Lingras, PhD Professor and Department Director of M.Sc. in Computing and Data Analytics And Mathematics and Computing Science | Saint Mary’s University Sreejata Chatterjee CEO & Co-Founder at HiVanya Derek Spinney, FCPA, FCMA VP Corporate Services, Infrastructure & CFO | Nova Scotia Health Pranay Malusare Data Analyst | Nova Scotia Power Kedar Gaikwad Automation AI Developer | The Citco Group Limited Fred Allen, MEd Professional Studies Manager | StFX

Instructor 2

About the instructor

Instructor 3

About the instructor

Instructor 4

About the instructor

Instructor 5

About the instructor

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