company-logo
services image
Pre-Launch

Market
Access Strategy

Launch

Day Zero
Planning

Lifecycle

Biosimilar
Simulation
Impact

...& Beyond

Literature Surveillance

Asset Scouting

Identifying Grants

Conference Coverage

Networking & Partnerships

Pipeline Databases

Drug Dev. Research

Market Access & Pricing

Knowledge Mining

Therapeutic Coverage

Commercial Organization Design

iconPre-Launch

GTM Strategy

Structured approach to launching and commercialising your asset balances regulatory compliance, market demand, pricing and access and competitive positioning to maximise commercial impact post-launch.

Commercial Assessments/Indication Prioritisation

Strategically optimise R&D investment, accelerate time-to-market, and maximise commercial success, ensuring that the most promising and impactful indications are pursued through robust analysis of unmet medical need, market potential, regulatory pathways, clinical feasibility, and competitive landscape.

Market Access Strategy

Demonstrate clinical efficacy, cost-effectiveness, and real-world benefits to healthcare providers, insurers, and policymakers. A strong market access strategy helps navigate regional regulations, formulary placements, and competitive dynamics, ensuring broad and sustainable patient access while maximising commercial success.

Publication Strategy

A well-executed publication strategy enhances brand reputation, educates stakeholders, and supports regulatory and market access efforts by demonstrating the drug's efficacy, safety, and value through strategic journal selection, conference and medical congresses attendance and publication alignment with commercialisation goals.

iconLaunch Phase

Launch Excellence

Ensure strategic execution to maximise adoption, patient access, and commercial success. Drive cross-functional collaboration across regulatory, market access, medical affairs, and commercial teams to ensure seamless execution and ensure data-driven, patient-centric growth and long-term impact in a competitive market.

Day-0 Planning

The preparation and strategic alignment needed to ensure a seamless market entry. Preparing regulatory readiness, market access approvals, stakeholder engagement, supply chain preparedness, and commercial strategy execution, including training sales teams, implementing omnichannel marketing campaigns. Effective Day 0 planning ensures that on launch day, the drug is available, accessible, and well-positioned for rapid uptake, driving early adoption and long-term success.

AI & Data Strategy

Prepare and execute a successful AI and data strategy, leveraging artificial intelligence (AI), machine learning (ML), Nature Language Processing (NLP) across multi modal inputs to promote enhanced diagnostic practices, treatment adherence & treatment outcomes, personalise marketing strategies and drive practice change.

iconLifecycle Optimisation

LoE Strategy

A well-planned LoE strategy helps sustain market share, maximise late-stage revenue, and extend your therapy's commercial impact beyond patent expiration due to generic or biosimilar competition. Critical examination of life cycle management (LCM) strategies should be prioritized. With an additional focus on Payer contracting, Real-world evidence (RWE) generation to maximise brand equity with Prescribers and Payers.

Digital Marketing Excellence

Drive Digital Marketing Excellence leveraging data-driven, omnichannel strategies to engage healthcare professionals (HCPs), patients, and payers effectively. It includes targeted content marketing, SEO, social media, email campaigns, webinars, and AI-powered personalisation to enhance awareness and adoption while ensuring compliance with regulatory guidelines. By utilizing real-time analytics, automation, and engagement tracking, pharma companies can optimize campaigns, improve customer experience, and drive brand loyalty, ultimately leading to better health outcomes and commercial success.

Business Development & Licensing

Continue the evolution of your portfolio, powering growth through seeking bolt-on opportunities via M&A, Strategic Partnership and Joint Ventures – all initiated with an asset scouting framework that characterizes the key components across Clinical and Commercial potential.

Therapeutic Areas

Specialised expertise across key therapeutic domains to drive successful product strategies

icon

Oncology

  • Non-Small Cell Lung Cancer
  • Breast Cancer (HER2 Negative, Positive & TNBC)
  • Ovarian Cancer
  • Endometrial Cancer
  • Prostate Cancer
  • Gastric Cancer
  • Colorectal & Esophageal Cancer
  • Liver Cancer
icon

Immunology

  • Rheumatoid Arthritis
  • Inflammatory Bowel Disease
  • Crohn's Disease
  • Psoriatic Arthritis
  • Lupus
icon

Ophthalmology

  • Neovascular age related macular degeneration (nAMD)
  • Diabetic Macular Edema (DME)
  • Retinal Vein Occlusion (RVO)
  • Dry AMD/Geographic Atrophy
icon

Neurology

  • Alzheimer's Disease
  • Multiple Sclerosis
icon

Cardio-Renal

  • Chronic Kidney Disease
  • Congestive Heart Failure
icon

Vaccines

  • Human papillomavirus (HPV)
  • Influenza A & B

Modalities

Comprehensive support across diverse treatment technologies to maximize commercial potential

    Monoclonal Antibodies (MABs)
  • Monoclonal Antibodies (MABs)
  • Cell and Gene Therapies
  • Cell and Gene Therapies
  • Antibody Drug Conjugates (ADCs)
  • Antibody Drug Conjugates (ADCs)
  • Radiotherapeutics (alpha, beta, gamma)
  • Radiotherapeutics (alpha, beta, gamma)
  • Antisense Molecules (siRNA, miRNA therapeutics)
  • Antisense Molecules (siRNA, miRNA therapeutics)
  • Small Molecules
  • Small Molecules
homepage end
Ready to lead your plan into the future?
Northwick Parntners Logo© 2024 Northwick Partners