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Contact : (321) 445-1969
To serve our clients in saving lives. It’s all about the patientsCONTACT US
We are an exclusive A-rated rescue organization empowered by the black belts of the biopharma. We are a focused disaster and rescue relief group of seasoned biopharmaceuticals professionals: Concentrating on major regulatory, clinical, medical, and/or operational disasters. We resolve significant findings, major 483, article 20's, consent decrees, the study holds, or safety/clinical- operational halts; no problem period CONTACT US
+ Read MoreWe manage the end- to- end rescue mission on any major challenges. We offer immediate pipeline expansions in case of failed trials, ramp up expansions, as needed, accrual boosting measures, as well as other boosting efforts to save the day. We are not just a group of consultants; we are a team of operatives. CONTACT US
A Strategic Consulting focused entirely on at-risk programs in the industry. Our clients are uniquely selected. Our leading staff colleagues are uniquely trained and skilled to execute the most challenging tasks at the toughest times of any organizations. The skilled and experienced subject matter experts are on-call 24/7. For questions Please CONTACT US
We are the real deal AI. While Oracle speaks of open data and cloud systems to
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Your Success is our mission.
Finally, we facilitate ready to in-licensee assets and programs as needed Should your company require pipeline, life cycle R & D development projects as well as a potential cash infusion to stay afloat? Read More
A Data Monitoring Committee (DMC) is an autonomous collection of clinical professionals which monitors patient safety andefficacy data
The CEC identifies/chartered suspected events by systematic review of clinical; including biomarkers related to the events of interest,
GAP begins a risk management program with classification and evaluation of risks related to the products.
(QPPV) services for clients who are entering in the European Union (EU) market to ensure a strong administration of Marketing Authorization Holder's
SCP- Technology is a novel modality that provides enhanced solubility of chemotherapeutic agents; in addition to the class III- IV compounds,
According to the new draft Drug Safety Guidance for Industry, Biopharmaceutical and Devices companies are urged to consider utilizing Safety Assessment Committees