We provide specialist services to the pharmaceutical industry
We are a flexible organisation with a team of experienced Biostatistics, Data Management, Statistical Programming, Medical Writing,
Pharmacovigilance, Safety and Regulatory Affairs. Professionals dedicated to providing high quality, practical, responsive, and cost-effective services to support biotechnology and pharmaceutical companies.
Which outsourcing solutions are you looking for?
Choose as many as you need.
Choose as many as you need.
About Sylphid Analytics
Sylphid Analytics is a global provider of specialized services to the pharmaceutical industry, offering high-quality, practical, responsive, and cost-effective solutions to support biotechnology and pharmaceutical companies. From Phase I to IV clinical trials, we expedite the development of life-saving drugs and devices, focusing on adaptability, quality, and efficiency throughout. Our commitment to excellence ensures that every client experiences complete confidence in our staff's knowledge, abilities, and reliability, witnessing clear benefits and results from our involvement in their projects. By supporting clients who facilitate the acceleration of drug approvals to market, we contribute to creating a safer and better world, shaping a brighter future for all.
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
