Statistical/Clinical SAS
Analysis Expertise

Tech Observer statistical services are composed of experienced Ph.D. and M.S. level of Statisticians/ Biostatisticians, SAS Certified Programmers. Read More

CDISC Compliance Expertise

Tech Observer has extensive experience in helping its customers become CDISC compliant. We have worked on large and small CDISC specific projects. Read More

Data Management Expertise

Tech Observerís dedicated Data Management experts provide accurate, regulatory-compliant clinical data solutions. Read More

EDC - Electronic Data Capture

Our secure and 21 CFR Part 11-compliant EDC system with its intuitive user interface is used to host your studies on-line.

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Pharmacovigilance and Drug Safety

Our services span the life cycle of marketed medical products, including pharmaceuticals, biologics and medical devices. Read More

Medical Writing Expertise

Our clinical writing process involves a sequence of scientific, statistical, editorial, managerial and quality control reviews at each developmental step. Read More

Quality Control/Assurance Expertise

Our QA team consists of senior auditors with expertise in Good Clinical Practice, Good Laboratory Practice, and Good Manufacturing Practice. Read More

Regulatory Affairs Expertise

Tech Observerís Regulatory Affairs Professionals are dedicated to ensuring the successful and timely submission of your application. Read More

Functional Service Provision (FSP) Expertise

Tech Observer is best known for its FSP whereby we become an extension of your clinical team through a combination of HR solutions. Read More

Clinical Monitoring Services Expertise

Our CRAs are assigned to specific sites for the duration of the study to provide consistent support for sites. Read More

Clinical, Healthcare And IT Staffing Services

We at Tech Observer employ a unique and effective recruiting strategy, which has the capability to reach not only the national resource pool but. Read More

About Tech Observer

We pride ourselves on our ability to provide innovative quality solutions to meet clinical challenges, all delivered RIGHT ON TIMEÖ.EVERY TIME.

Our industry-standard, validated SAS and data management system, compliant with ICH GCP guidelines and 21 CFR Part 11 regulations is a guarantee that you will always be provided with data of the highest quality.

Recent News

Jun 07, 2016
Come & Meet us @ China Medical Affairs Summit
We're in Shanghai, China for the China Medical Affairs Summit, and we're looking forward to the great time with people from healthcare fraternity . Come find us at booth...

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