Ceutical Laboratories, Inc.

assainternational® was established in 1999 as a think tank and analytical resource to the pharmaceutical industry. Our mission is to offer international expertise in the many facets of solid-state characterization of pharmaceutical solids. As well as being a valued independent resource, we offer a variety of services that support the most current and up-to-date developments, innovations and technology.

assa® offers outstanding workshops and conferences on solid-state characterization of pharmaceutical material. The International Workshop on Solid-State Characterization of Pharmaceutical Solids (IWPCPS®) is known worldwide as the most comprehensive and up-to-date workshop of it’s kind.

assa® offers solid-state characterization of substances and formulations. We cover the whole range from early discovery phase to marketed products. We can also offer a unique inhalation know how.

Protecting intellectual property rights is one of the most critical tasks in pharmaceutical R&D. We work with international law firms to address your needs.

We can also assist you with setting up a complete, modern, solid-state characterization laboratory and provide assistance with the qualification or adherence (accreditation) of your laboratory to regulatory compliance codes.

assa® offers Business Services in marketing and sales issues to support the pharmaceutical industry, and all adjunct and related companies in related fields.

Amarex is a global, full-service Contract Research Organization (CRO), whose leadership team has significant expertise conducting biomedical research, and whose combined experience includes the design and conduct of several hundred clinical research projects in many therapeutic indications. Amarex provides comprehensive services in Project Management (Phase I-IV, BE/BA, PK/PD), Regulatory Affairs (FDA Applications and meetings, Applications to International Health Authorities, GxP Compliance Audits), Clinical Operations, Adaptive Study Designs, Statistical Analysis, Data Management, Medical Monitoring, Safety and Pharmacovigilance, and General Consulting. Amarex can take your product through the entire approval process, from creating the regulatory approval strategy, to conducting trials, to writing the marketing approval application. Join our growing list of clients with approved products. Amarex provides high quality and cost efficient services.

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ClinDatrix is a privately held, full-service contract research organization (CRO) founded in 2002 to help drug and medical device innovators advance their therapeutic products toward regulatory approval. Over the past decade, ClinDatrix has grown to offer contract research expertise from preclinical development guidance through regulatory filings and post-marketing studies. We continue to work primarily with small to mid-sized companies, a subset of innovators we know and serve very well. We also are a reliable resource to large pharma and medical device companies seeking to outsource specialized tasks for timely completion.

Clinlogix is a Global Clinical Research Service & Consulting Organization working to improve human quality of life by supporting innovation in the life science industry. Its full suite of clinical research services supports the regulatory and clinical development pathway of medical devices, pharmaceuticals, biologics and diagnostics from proof of concept/discovery, early feasibility/first-in-human, through pivotal and the post-marketing/safety surveillance of client products. The company delivers this global expertise by way of its regional office locations in the US - Spring House, Pennsylvania, Europe - Mainz, Germany, Latin America - Medellin, Colombia and Asia Pacific - Tokyo, Japan.

Cromos Pharma is an international CRO with expertise in delivering all aspects of clinical trials in all clinical phases and a range of therapeutic areas.

Cromos Pharma offers fully integrated CRO services including regulatory consulting and compliance, project management; monitoring; medical writing; data management and biostatistics; drug and device registration services; logistics and warehousing; post-marketing services and independent audits. Cromos Pharma delivers rapid recruitment and excellent patient retention as well as expert study design and management.

Cromos Pharma's "No Patients - No Payments"​ initiative allows the sponsors to pay for performance and is our guarantee that the study timelines will be met.

Established in Moscow in 2004, Cromos Pharma has strong regional presences in Central and Eastern Europe, Russia and Post-Soviet Bloc countries. Its European HQ is situated in Dublin, Ireland and its US base is in Portland, Oregon.