Biostatistics plays an important role in the field of pharmaceutical and healthcare industries especially in Clinical trials and drug development. Abiogenesis Clinpharm provides a team of biostatistics for comprehensive services to support clinical trial needs. We have experienced biostatisticians to ensure that the data are analyzed, interpreted and reported with accuracy and integrity. Our expertise work closely with clients to ensure seamless project execution and timely delivery.

The biostatistics department of Abiogenesis Clinpharm offers a range of services from statistical input in protocol development to analysis and report preparation. Our team collaborates with data management and medical writing team at every stage ensuring successful high quality delivery of clinical development program. Abiogenesis Clinpharm have a Biostatistics Lead, Senior Biostatistics and numerous SAS Programmers who work at entry level to senior level.

Biostatistical Services

Biostatisticians in Contract Research Organization design the clinical trials. They determine sample size and randomized strategies to ensure that the study yields reliable and authentic results.

 At Abiogenesis Clinpharm, our biostatistics team assists in designing studies to align with research goals and develop protocols ensuring accurate data collection and analysis.

In clinical trials, randomization is crucial to ensure even distribution of participants, integrity and validity of clinical trials. Our biostatistics team prepares the randomization plan based on study design and objectives. This enables our researchers to draw significant differences statistically enhancing statistical power of the study.

Our data expert managers and biostatisticians collect clinical trial data accurately and manage and analyze the data for drug development plans. At Abiogenesis, our team uses various statistical techniques to analyze the collected data from clinical trials to understand the safety and efficacy of innovative measures.

Our biostatisticians are capable of providing expertise to design and develop CRFs and eCRFs for clinical trials for accurate and complete data collection. Our input in CRFs and eCRFs development ensures high quality data enhancing data management and analysis efficiency in compliance with regulatory requirements.

At Abiogenesis Clinpharm, our team uses statistical SAS Programming languages to extract efficient and meaningful insights from clinical trial data. We apply advanced statistical techniques to provide information for drug development and regulatory decisions.

Our biostatistics team provides expertise in both clinical and regulatory biostatistics to ensure that our clients receive complete support. Our Statistical Programming Services enables accurate and efficient outcomes from study design to data analysis.

Our biostatisticians prepare regulatory data for submissions to regulatory bodies like the FDA and EMA and create reports that adhere to legal specifications. Our team can effectively communicate complex statistical findings in a simple and concise manner that meets all regulatory requirements.

Our team are experts in providing comprehensive review and audit services, ensuring high data quality and integrity. Abiogenesis Clinpharm provides accurate and reliable data in all phases of Clinical trials process. Our reports give a comprehensive overview in a clear, simple, and well-documented manner of data quality and protocol adherence.

At Abiogenesis Clinpharm, our biostatistics team provides an extensive and proficient biostatistical services for clinical trial to deliver a high quality services with a solid foundation in biostatistics and clinical research. Our team are expertise in analyzing and interpreting data in various therapeutic area managing a range of biostatistics and programming activities including statistical tables, graphs and determination of primary and secondary end points. Our biostatistics team collaborates closely with clients to comprehend every aspect of their needs to assure smooth project execution in compliance with regulatory requirements.

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