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    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.

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    Full-Service CRO Integrated Solutions That Accelerate Drug Development

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

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    Lambda-Novum Global Corporate Presentation

    Full-Service CRO Integrated Solutions That Accelerate Drug Development

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

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    Lambda-Novum Global Corporate Presentation

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    Therapeutic Expertise

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

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

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

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    Strategic Endpoint Selection for Successful Oncology Clinical Trials

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

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

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    Strategic Endpoint Selection for Successful Oncology Clinical Trials

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    Audit and inspection readiness - Comprehensive Approach - Lambda Therapeutic Research

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

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

    Bioequivalence Study of Semaglutide Injection (GLP-1 analogue)

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

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    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.

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

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    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

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    Lambda Successfully Completes US FDA Pharmacovigilance Inspection with Zero 483s

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

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    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

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    Lambda Successfully Completes US FDA Pharmacovigilance Inspection with Zero 483s

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

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    Meeting MI & PV Obligations for a COVID-19 Vaccine

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

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    AI in Clinical Trial: Present and Future

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

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    Meeting MI & PV Obligations for a COVID-19 Vaccine

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

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    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
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    Overcoming Challenges in a Multicenter Oncology Clinical Trial - Lambda Therapeutic Research - Top CRO - Leading CRO

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    Overcoming Challenges in a Multicenter Oncology Clinical Trial

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    From Logistics to Seamless Analysis : Enhancing Medical Imaging

    Quality assurance team ensuring compliance and reliability in clinical research

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    Overcoming Challenges in a Multicenter Oncology Clinical Trial

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    From Logistics to Seamless Analysis : Enhancing Medical Imaging

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  • 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

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    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

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    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

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    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

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    Lambda Therapeutic Research wins back-to-back global awards

You are currently viewing 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

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Recent Posts

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  • Clinical Insights from a Bioequivalence Study of Pertuzumab 420 mg Solution for Infusion
  • Bioanalytical Assays – Methods Library
  • Qualified Person for Pharmacovigilance (QPPV): Strengthening Compliance Across the EU and UK
  • Enrollment Excellence in Phase-3 Semaglutide Trials – 514 Patients in Just 2 Months

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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

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  • Early Phase
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Therapeutic Expertise

  • Oncology & Hematology CRO
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  • Pulmonology CRO
  • Cardiovascular & Metabolic disorders
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