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    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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    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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    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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    Audit and inspection readiness - Comprehensive Approach - Lambda Therapeutic Research

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

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

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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
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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

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    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
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    • Neuroscience
    • Biosimilar Development
    • Infectious Disease
    • Pulmonology
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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

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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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    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
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    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 >

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    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

Read more about the article A highly complex, sensitive and simultaneous LC-MS/MS method for the quantification of Total Estrone and Equilin in human plasma
A highly complex, sensitive and simultaneous LC-MS/MS method for the quantification of Total Estrone & Total Equilin in human plasma

A highly complex, sensitive and simultaneous LC-MS/MS method for the quantification of Total Estrone and Equilin in human plasma

  • Post author:Dipesh Chodvadia
  • Post published:August 21, 2023
  • Post category:Blog/Labs

Blog

Continue ReadingA highly complex, sensitive and simultaneous LC-MS/MS method for the quantification of Total Estrone and Equilin in human plasma

Recent Posts

  • Bioanalytical Methods / Assay List (Lambda & Novum)
  • Study Insights: Phase-I, Bioequivalence Study of Trastuzumab SC Injection
  • Specialized Clinical Development Support for Semaglutide Programs
  • Bioanalytical Excellence Upheld – Unannounced US FDA inspection concludes with Zero 483s
  • Lambda Successfully Completes US FDA Pharmacovigilance Inspection with Zero 483s – 4th Consecutive in One Year

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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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