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  • Capabilities

    Capabilities

    Our capabilities extend across the entire spectrum of clinical research services, providing end-to-end solutions for the successful development of your innovative therapies.

    Overview >

    • Strategic Product Development & Consulting
    • Early development and innovation
    • Phase II-IV Clinical Trial Management
    • Clinical Development Services (CDS) Project Management
    • Regulatory Affairs
    • Medical Writing
    • CDMO Services
    • Biostatistics & Data Management
    • Medical Affairs
    • Clinical Safety & Pharmacovigilance
    • Medical Imaging
    • eTMF
    • Quality Assurance
    • Technology
    • Labs
    Full-Service CRO Integrated Solutions That Accelerate Drug Development

    BLOG

    Full-Service CRO | End-to-End Expertise for Every Phase of Clinical Development

    PDF

    Lambda-Novum Global Corporate Presentation

    Full-Service CRO Integrated Solutions That Accelerate Drug Development

    BLOG

    Full-Service CRO | End-to-End Expertise for Every Phase of Clinical Development

    PDF

    Lambda-Novum Global Corporate Presentation

  • Therapeutic Expertise

    Therapeutic Expertise

    Empowering innovation and advancing vital therapies across diverse therapeutic areas, with extensive experience supporting over 265+ clinical trials across 15+ therapeutic domains.

    Overview >

    • Oncology & Hematology
    • Dermatology
    • Neuroscience
    • Biosimilar Development
    • Infectious Disease
    • Pulmonology
    • Cardiovascular & Metabolic disorder
    • Gastroenterology
    • Nephrology
    • Ophthalmology
    • Musculoskeletal
    • Cross-Therapeutic
    Accelerating Patient Recruitment in Ranibizumab Study for Retinopathy of Prematurity in Preterm Infants

    CASE-STUDY

    CONQUERING COMPLEX STUDIES: Accelerating Patient Recruitment in Ranibizumab Study for Retinopathy of Prematurity in Preterm Infants

    Strategic Endpoint Selection for Successful Oncology Trials - CRO

    Blog

    Strategic Endpoint Selection for Successful Oncology Clinical Trials

    Accelerating Patient Recruitment in Ranibizumab Study for Retinopathy of Prematurity in Preterm Infants

    CASE-STUDY

    CONQUERING COMPLEX STUDIES: Accelerating Patient Recruitment in Ranibizumab Study for Retinopathy of Prematurity in Preterm Infants

    Strategic Endpoint Selection for Successful Oncology Trials - CRO

    Blog

    Strategic Endpoint Selection for Successful Oncology Clinical Trials

  • Labs
  • Imaging
  • Phase-I Unit
  • Insights

    Insights

    Leveraging decades of clinical research expertise, global compliance, and therapeutic experience, we are committed to ensuring the seamless progress of your promising therapy.

    Overview >

    • Research Blogs
    • Resource Center
    • Newsletter
    • Case-Study
    • Clinical Research Update
    • Service and Capabilities

    Insights

    Audit and Inspection Readiness: A Comprehensive Approach

    Case study - From Operational Strain to Compliance - PV Transformation for a Global Pharma Client

    Case-study

    From Operational Strain to Compliance – PV Transformation for Global Pharma Client

    Case-study

    Bioequivalence Study of Semaglutide Injection 1.34 mg/ml (2 mg/1.5 mL)

  • About

    Our Presence

    Leveraging decades of clinical research expertise, global compliance, and therapeutic experience, we are committed to ensuring the seamless progress of your promising therapy.

    Overview >

    • Our Approach
    • Trusted by Biotech and Pharma
    • Leadership
    • Advisory Board
    • Corporate Social Responsibility Initiatives
    • Regulatory Compliance
    • News
    • Events
    • Locations
    • Life at Lambda
    • Contact
    Bioanalytical Excellence Upheld - Unannounced US FDA inspection concludes with Zero 483s - Lambda CRO

    NEWS

    Bioanalytical Excellence Upheld – Unannounced US FDA inspection concludes with Zero 483s

    Lambda Clears 4 Back-to-Back US FDA PV Inspections in 12 Months Without 483s

    NEWS

    Lambda Successfully Completes US FDA Pharmacovigilance Inspection with Zero 483s

    Bioanalytical Excellence Upheld - Unannounced US FDA inspection concludes with Zero 483s - Lambda CRO

    News

    Bioanalytical Excellence Upheld – Unannounced US FDA inspection concludes with Zero 483s

    Lambda Clears 4 Back-to-Back US FDA PV Inspections in 12 Months Without 483s

    News

    Lambda Successfully Completes US FDA Pharmacovigilance Inspection with Zero 483s

Novum Pharmaceutical Research Logo
Lambda Therapeutic Research Logo
  • Capabilities

    Our Capabilities

    Our capabilities extend across the entire spectrum of clinical research services, providing end-to-end solutions for the successful development of your innovative therapies.

    Overview >

    • Strategic Product Development & Consulting
    • Early development and innovation
    • Phase II-IV Clinical Trial Management
    • Clinical Development Services (CDS) Project Management
    • Regulatory Affairs
    • Medical Writing
    • Technology
    • CDMO Services
    • Biostatistics & Data Management
    • Medical Affairs
    • Clinical Safety & Pharmacovigilance
    • Medical Imaging
    • eTMF
    • Quality Assurance
    • Labs
    Blog: Clinical Safety & Pharmacovigilance - Meeting MI & PV Obligations for a COVID-19 Vaccine

    BLOG

    Meeting MI & PV Obligations for a COVID-19 Vaccine

    AI in Clinical Trial: Present and Future - Lambda Therapeutic Research

    BLOG

    AI in Clinical Trial: Present and Future

    Blog: Clinical Safety & Pharmacovigilance - Meeting MI & PV Obligations for a COVID-19 Vaccine

    BLOG

    Meeting MI & PV Obligations for a COVID-19 Vaccine

    AI in Clinical Trial: Present and Future - Lambda Therapeutic Research

    BLOG

    AI in Clinical Trial: Present and Future

  • Therapeutic Expertise

    Therapeutic Expertise

    Empowering innovation and advancing vital therapies across diverse therapeutic areas, with extensive experience supporting over 280+ clinical trials across 15+ therapeutic domains.

    Overview >

    • Oncology & Hematology
    • Dermatology
    • Neuroscience
    • Biosimilar Development
    • Infectious Disease
    • Pulmonology
    • Cardiovascular & Metabolic disorder
    • Gastroenterology
    • Nephrology
    • Ophthalmology
    • Musculoskeletal
    • Cross-Therapeutic
    Overcoming Challenges in a Multicenter Oncology Clinical Trial - Lambda Therapeutic Research - Top CRO - Leading CRO

    CASE-STUDY

    Overcoming Challenges in a Multicenter Oncology Clinical Trial

    CASE-STUDY

    From Logistics to Seamless Analysis : Enhancing Medical Imaging

    Quality assurance team ensuring compliance and reliability in clinical research

    CASE-STUDY

    Overcoming Challenges in a Multicenter Oncology Clinical Trial

    CASE-STUDY

    From Logistics to Seamless Analysis : Enhancing Medical Imaging

  • Labs
  • Imaging
  • Phase-I Unit
  • Insights

    Insights

    Leveraging decades of clinical research expertise, global compliance, and therapeutic experience, we are committed to ensuring the seamless progress of your promising therapy.

    Overview >

    • Research Blogs
    • Resource Center
    • Newsletter
    • Case-Study
    • Clinical Research Update
    • Service and Capabilities

    Insights

    Audit and Inspection Readiness: A Comprehensive Approach

    Case study - From Operational Strain to Compliance - PV Transformation for a Global Pharma Client

    Case-study

    From Operational Strain to Compliance – PV Transformation for Global Pharma Client

    Case-study

    Bioequivalence Study of Semaglutide Injection 1.34 mg/ml (2 mg/1.5 mL)

  • About

    Our Presence

    Leveraging decades of clinical research expertise, global compliance, and therapeutic experience, we are committed to ensuring the seamless progress of your promising therapy.

    Overview >

    • Our Approach
    • Trusted by Biotech and Pharma
    • Leadership
    • Advisory Board
    • Corporate Social Responsibility Initiatives
    • Regulatory Compliance
    • News
    • Events
    • Locations
    • Life at Lambda
    • Contact
    Lambda Therapeutic Research Wins Global Awards: CPHI and GGB Awards 2023

    NEWS

    Lambda wins back-to-back global awards at CPHI and GGB.

    Lambda’s BA-BE Centre in India Successfully Passes GCC Inspection with Zero Observations

    NEWS

    Lambda's BA-BE Centre in India Successfully Passes GCC Inspection..

    Lambda’s BA-BE Centre in India Successfully Passes GCC Inspection with Zero Observations

    NEWS

    Lambda's BA-BE Centre in India Successfully Passes GCC Inspection..

    Lambda’s success with the prestigious ‘Industry Partner of the Year’ Award at the Global Generics & Biosimilar Awards 2023 in Barcelona on October 25, 2023

    NEWS

    Lambda Therapeutic Research wins back-to-back global awards

Read more about the article Ovarian Cancer Clinical Trials – Advancing Research Through Patient-Focused Approaches
Ovarian Cancer Clinical Trials CRO India USA

Ovarian Cancer Clinical Trials – Advancing Research Through Patient-Focused Approaches

  • Post author:Dipesh Chodvadia
  • Post published:May 8, 2025
  • Post category:Blog/Late Phase

Blog

Continue ReadingOvarian Cancer Clinical Trials – Advancing Research Through Patient-Focused Approaches
Read more about the article End-to-end Biosimilar Development and Clinical Trials Expertise
Lambda CRO - End-to-end Biosimilar Development and Clinical Trials Expertise

End-to-end Biosimilar Development and Clinical Trials Expertise

  • Post author:Dipesh Chodvadia
  • Post published:May 1, 2025
  • Post category:Biosimilar/Services & Capabilities

Continue ReadingEnd-to-end Biosimilar Development and Clinical Trials Expertise
Read more about the article Advancing Late Phase Clinical Trials
Lambda - Advancing Clinical Trials - Global Full-service CRO

Advancing Late Phase Clinical Trials

  • Post author:Dipesh Chodvadia
  • Post published:May 1, 2025
  • Post category:Late Phase/Services & Capabilities

Continue ReadingAdvancing Late Phase Clinical Trials
Read more about the article Strategic Endpoint Selection for Successful Oncology Clinical Trials
Strategic Endpoint Selection for Successful Oncology Trials - CRO

Strategic Endpoint Selection for Successful Oncology Clinical Trials

  • Post author:Dipesh Chodvadia
  • Post published:April 29, 2025
  • Post category:Blog/Late Phase

Blog

Continue ReadingStrategic Endpoint Selection for Successful Oncology Clinical Trials
Read more about the article Navigating CDSCO Regulations: Key Approval Processes and Lambda’s Regulatory Support
Navigating CDSCO Regulations: Key Approval Processes & Lambda's Regulatory Support

Navigating CDSCO Regulations: Key Approval Processes and Lambda’s Regulatory Support

  • Post author:Dipesh Chodvadia
  • Post published:April 23, 2025
  • Post category:Blog/Clinical Research

Blog

Continue ReadingNavigating CDSCO Regulations: Key Approval Processes and Lambda’s Regulatory Support
Read more about the article Advancing Clinical Development in Women’s Health
Advancing Clinical Development in Women’s Health - Lambda-Novum CRO

Advancing Clinical Development in Women’s Health

  • Post author:Dipesh Chodvadia
  • Post published:April 16, 2025
  • Post category:Blog/Late Phase

Blog

Continue ReadingAdvancing Clinical Development in Women’s Health
Read more about the article A Highly Precise, Accurate, and Robust LC-MS/MS Method for the Quantification of Semaglutide in Human Plasma
A Highly Precise, Accurate, and Robust LC-MSMS Method for the Quantification of Semaglutide in Human Plasma

A Highly Precise, Accurate, and Robust LC-MS/MS Method for the Quantification of Semaglutide in Human Plasma

  • Post author:Dipesh Chodvadia
  • Post published:March 26, 2025
  • Post category:Blog/Labs

Blog

Continue ReadingA Highly Precise, Accurate, and Robust LC-MS/MS Method for the Quantification of Semaglutide in Human Plasma
Read more about the article Ensuring Drug Safety: Lambda’s Pharmacovigilance Milestones in 2024
Ensuring Drug Safety Lambda’s Pharmacovigilance Milestones in 2024

Ensuring Drug Safety: Lambda’s Pharmacovigilance Milestones in 2024

  • Post author:Dipesh Chodvadia
  • Post published:January 31, 2025
  • Post category:Blog/Pharmacovigilance

BLOG

Continue ReadingEnsuring Drug Safety: Lambda’s Pharmacovigilance Milestones in 2024
Read more about the article Nutraceuticals and Consumer Products Studies: Ensure product safety & efficacy with expert-led trials
Nutraceuticals and Consumer Products CRO - Ensure product safety and efficacy with expert-led Clinical trials

Nutraceuticals and Consumer Products Studies: Ensure product safety & efficacy with expert-led trials

  • Post author:Dipesh Chodvadia
  • Post published:December 25, 2024
  • Post category:Blog/Early Phase

Blog

Continue ReadingNutraceuticals and Consumer Products Studies: Ensure product safety & efficacy with expert-led trials
Read more about the article Advancing Prostate Cancer Clinical Trials: Key Insights
Advancing Prostate Cancer Clinical Trials - Lambda CRO - India, USA, Canada

Advancing Prostate Cancer Clinical Trials: Key Insights

  • Post author:Dipesh Chodvadia
  • Post published:December 17, 2024
  • Post category:Blog/Late Phase

Blog

Continue ReadingAdvancing Prostate Cancer Clinical Trials: Key Insights
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Recent Posts

  • Patient-Centric Trials in Advancing Cancer Research: A Journey of Progress & Hope
  • EMA and FDA Publish Common Principles for AI in Drug Development
  • Regulatory Developments That Shaped Clinical Trials in 2025
  • From Compliance to Confidence – Lambda Pharmacovigilance Milestones 2025
  • Specialized Clinical Development Support for Semaglutide Programs

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Lambda Therapeutic Research Logo

Lambda Therapeutic Research is a Global full-service Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK) and Warsaw (Poland), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries.

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Capabilities

  • Strategic Product Development
  • Early Phase
  • Late Phase
  • Clinical Development Services
  • Biostatistics & Data Management
  • Medical Affairs
  • Pharmacovigilance
  • Medical Imaging
  • Regulatory Affairs
  • Medical Writing
  • Quality Assurance
  • Bioanalytical & Biosimilar Lab
  • Central Clinical Lab
  • Technology
  • CDMO Services

Therapeutic Expertise

  • Oncology & Hematology CRO
  • Dermatology CRO
  • Neurology & Psychiatry CRO
  • Biosimilar Development CRO
  • Infectious Disease & Vaccines CRO
  • Pulmonology CRO
  • Cardiovascular & Metabolic disorders
  • Gastroenterology CRO
  • Nephrology CRO
  • Ophthalmology CRO
  • Musculoskeletal CRO
  • Cell & gene therapies CRO
  • Nutraceuticals CRO
  • Pediatrics CRO
  • Women's Health CRO

Company

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  • Leadership
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  • Regulatory Compliance
  • News
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  • Contact

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