DebLink Research LLC
Accelerate Drug/Device Approval
By Prioritizing Patient Safety, Data Integrity, and Regulatory Compliance in All Aspect of Drug Development Process
DebLink Research LLC is a Chicago-based firm offering a comprehensive range of services in drug development research. Our team comprises industry experts with a deep understanding of the complex regulatory landscape, and we provide support to clients at every stage of the drug development process.
Our services begin with preclinical research, which is a crucial phase in the drug development process. During this stage, our team works closely with clients to conduct studies that test the safety and efficacy of potential drugs in animal models. Our preclinical studies follow industry standards and regulatory requirements, ensuring that the results are robust and reliable.
Once the preclinical studies are complete, the next step is to submit an Investigational New Drug (IND) application to the FDA. This is where our experience in drug development comes into play. We have a thorough understanding of the IND application process and can guide clients through the steps required to obtain FDA approval to move on to clinical trials.
OUR SCOPE
Therapeutic Areas:
Cardiovascular
Oncology
CNS
Epilepsy, Alzheimer, Stroke, Meningitis, Encephalitis, Parkinson’s disease
Ophthalmology
Open-Angle Glaukoma, Dry Eye Disease, Keratoconus, Blepharitis
Respiratory
COVID-19, Asthma, Pneumonia, Bronchitis
Orthopedics
Osteoperosis, Rheumatoid Athritis, Shoulder Athroplasty
In-Vitro Diagnostics
Vaccines, Hepatitis B, Hepatitis C, Cardiology
Urology
UTI, Hematuria, Erectile Dysfunction
Dermatology
Acne, Atopic Dermatitis, Shingles
GI
GERD, Irritable Bowel Syndrom, Colonoscopy
Infectious Disease
COVID-19, The Flu (Influenza), HSV-1 and HSV-2, HIV
What is DebLink Research
Mission
To enable our clients improve patients’ lives through innovative drug and medical device development using safe, effective, efficient, and ethical methods.
Our Clients includes:
- Sponsors
- CROs
- Study Sites
WHAT WE PROVIDE
Our Solutions
Phase I-IV Clinical Trial Management
Class I-III Medical Device Submissions
SOP Development/Implementation
Staffing/ Talent Recruitment
Clinical Audits: Sites, CROs and Sponsor
PIR: Proficiency in Research Training Program
Data Management
Pharmacovigilance
Contracts
TESTIMONIALS
Some feedbacks from our clients
We deliver our deliverables to our clients at the highest quality. Our team is highly effective, efficient, and value client satisfaction.