Life Science Consulting

Life Sciences Consulting Services

The Life Science industry is constantly changing. Technology improves, medicines and therapies advance, and new regulations emerge. When gaps occur, our Life Sciences & Technology group moves swiftly to provide professionals who can adapt to those changes and ensure that companies are in compliance today and in the future.

Logik Scienes provides clinical research and development services to pharmaceutical, biotechnology and medical device clients worldwide, supporting our clients in their drug discovery and development work.

Independently owned, our expertise supports the full spectrum of contract clinical research – from phase I-IV studies.

Backed by extensive expertise to support regulatory filings, drug safety and QA, our accredited laboratories provide dedicated clinical pathology, microbiology and bio-analytical services.

Focused on clinical success, we are committed to our clients’ safe, efficient and successful drug development.

Clinical R & D

We understand that research and development is critical to addressing health needs and improving lives. To help you fulfill your passion for helping others, we will match you with R & D jobs that allow you to keep your skills sharp and grow within your functional area. We specialize in placing experts in clinical research jobs across a broad range of therapeutic areas and all phases of development.

• Clinical Operations
• Medical Writing
• Biometrics
• Pharmacovigilance
• Regulatory Affairs
• Quality Assurance – GCP

Data  Integrity

Logik Sciences helps businesses mitigate data integrity issues to meet regulatory compliance, improve quality operations and create a platform for evidence-based decision making.

Phase IIb/III/IV studies

• Fast-track patient recruitment for late stage marketing trials
• Special patient populations easily accessible and rapidly recruited
• Trusted network of General Practitioners and hospital consultants
• Dedicated project management for each study

Enjoy peace of mind – our expertise and efficiency delivers RoI for every client, every time. Regulatory services

• Drug safety and pharmacovigiliance
• Regulatory filing, advice and guidance
• Biometrics and data management
• Protocol and case report design
• Report creation and medical writing
• Quality assurance
• Fully accredited laboratory (GLP, CPA, ISO9002)
• Trusted partners enable us to access pre-clinical toxicology, rapid bio-analytical techniques, validated bio-markers, bio-discovery and sample logistics

Investigational Site Monitoring Services

Investigational Site Monitoring is a crucial aspect of any Clinical Trial. Our professional CRAs, Lead CRAs and CTAs can manage all of your site visits, such as Pre-study (PSV), Site initiation (SIV), interim monitoring (IMV) and close-out (COV) visits. Trust our team to monitor your clinical trials!