Trusted Clinical Research Partner for Pharmaceutical & Biotechnology Companies
We are a flexible and client-focused organization with experienced professionals in Biostatistics, Data Management, Statistical Programming, Medical Writing, Pharmacovigilance, Safety, and Regulatory Affairs.
We deliver high-quality, practical, responsive, and cost-effective solutions that help pharmaceutical and biotechnology companies accelerate development with confidence.
We deliver high-quality, practical, responsive, and cost-effective solutions that help pharmaceutical and biotechnology companies accelerate development with confidence.
Explore Our Clinical Research Service Expertise
Flexible engagement models tailored to your project needs.
Flexible engagement models tailored to your project needs.
About Sylphid Analytics
Sylphid Analytics is a trusted global provider of specialized clinical research services for pharmaceutical and biotechnology companies.
We support Phase I to Phase IV clinical trials through high-quality, responsive, and cost-effective solutions across biostatistics, data management, statistical programming, medical writing, pharmacovigilance, and regulatory affairs.
Our agile approach helps clients accelerate drug development timelines, maintain compliance, and bring life-changing therapies to market faster.
With a commitment to quality, reliability, and scientific excellence, we build long-term partnerships that deliver measurable results.
We support Phase I to Phase IV clinical trials through high-quality, responsive, and cost-effective solutions across biostatistics, data management, statistical programming, medical writing, pharmacovigilance, and regulatory affairs.
Our agile approach helps clients accelerate drug development timelines, maintain compliance, and bring life-changing therapies to market faster.
With a commitment to quality, reliability, and scientific excellence, we build long-term partnerships that deliver measurable results.
Sharing Success Stories
Biostatistics
Our Biostatistician services are designed to be your dedicated partner for achieving precision in every aspect of clinical research projects.
With a focus on innovative study designs, effective randomization
processes, and thorough data analyses, we ensure the reliability of your results and provide clear
interpretation through comprehensive statistical analysis plans. Our commitment extends to generating
detailed statistical reports, contributing to Clinical Study Reports, and leveraging cutting-edge
technology for accurate and timely data analysis.
Protocol development
Study design
Power calculations
Statistical Programming
At Sylphid, we take pride in being your comprehensive SAS programming partner for clinical research.
Our seasoned team of SAS programmers is dedicated to delivering top-tier services, covering a spectrum of needs, including CDISC standards implementation, legacy services, and expertise across various therapeutic areas. Our SAS programmers possess a wealth of experience in clinical research, ensuring that our solutions meet the rigorous demands of the industry. We are committed to staying abreast of the latest developments and best practices to deliver cutting-edge programming services.
Oncology
Cardiovascular
Infectious Diseases
Clinical Data Management
In the dynamic landscape of the clinical industry, our solutions cater to biopharmaceutical, biotech, and medical device companies, emphasizing data integrity and employing innovative technologies. Our skilled teams, adhering to ICH E6 R2 guidelines, excel in clinical data management activities—from designing eCRFs to delivering accurate datasets for statistical analysis. With a commitment to quality and regulatory compliance, we prioritize clean and reliable data, fostering strong customer relationships through professionalism, flexibility, and exceptional expertise in therapeutic and regulatory domains.
Data Management Plan
Validation of Data
Database Design
Pharmacovigilance
We provide a wide range of high-quality global Pharmacovigilance/safety solutions. We have operationally excelled teams to provide customized solutions across the Good Pharmacovigilance Practice (GVP) in relevant health authority requirements.
PLPA/Compassionate use
Signal detection
Medical Writing
Our extensive medical writing services are supported by a wide range of knowledge in therapeutic areas and document expertise, customized to meet your project and regulatory requirements and deliver high-quality and scientifically rigorous medical writing deliverables to support your clinical development.
Utilizing practical experience and up-to-date regulatory knowledge, our writers provide expertise in navigating differing global requirements and delivering a collaborative partnership.
Study Design
brochure
Informed Consent Forms
Regulatory Affairs
Our regulatory team has everything you need to achieve successful agency dialogue, plan your
regulatory strategy, achieve timely submissions and approvals. Whatever your regulatory need, we
are here to help.
R&D / Development Phase
Marketing Authorisation/Registration
