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Site en français                                                                                                                                         Blog: Early-Clinical-Research


CONTRACT RESEARCH ORGANIZATION: First-in-man, Phase I and Bioequivalence clinical studies.

ALS is a leading world-class CRO, offering solutions and Strategies that speed the product clinical development up. Read the testimonies about ALS Professionals, a team that Pharmaceuticals and Biotech can trust and rely on. From a glance of viewing our e-Library, it can be seen that each clinical study deserves a deep due diligence: it is designed and accomplished through an extensive review of available data, literature and guidance.

We conducted a variety of clinical studies driven by Ethics, Guidance and an extensive review of literature:
- Phase 0 / Micro-dosing / First-in-man clinical trials
- Phase I (phase 1) clinical trials
- Bioavailability / Bioequivalence (BA/BE) clinical studies
- Nutraceutical clinical studies that we approach with rigor and specific guidance.


We have the expertise and the experience required for the following therapeutic areas but not limited to:
- Allergies, Alzheimer, Cardiovascular, Depression, Diabetes, Epilepsy, Gastro-enterology, Hormones, Immunology, Oncology, Osteoporosis, Pain killers, Parkinson, Influenza virus vaccine.
- Natural health products, functional foods, probiotics.

- We are expert in the clinical development process of pharmaceutical drug products, biologics and medical devices.
- We help pharmaceuticals and biotech with input, support and writing of white papers: publication of study results, graphical presentations for press-release, business plan, funds raising, claim of SR&ED expenses of studies conducted with us, meetings with investors.
- Our expertise of Phase I clinical trials is an asset for complex bioequivalence clinical studies.
- We use an integrated and secured database and a-24/7 service for reliable and timely subject recruitment. The database contains healthy volunteers and a list of special populations. With our multilingual staff, the study subjects are well informed about the study rules, their rights and their obligations.
- Our clinical studies are conducted in collaboration with qualified GLP labs for OTC, Rx medications, Herbal & Natural Medicines. To view the validated analytical methods, click''here''.
- Visit our facilities: Link 1 - Link 2

Should you require any information, we'll be pleased to assisting you: call 1 514 750 6017 or write ''Email''.

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