 |
|
|
Leading Preclinical
CRO Management
Tough times require tough decisions; those decisions require experience. VIDA Sciences brings more than 50 years in the preclinical contract research organization (CRO) industry, including senior leadership positions, that are invaluable to CROs.
Our CEO, Bill Harrison, is an internationally recognized expert in preclinical CRO management and Good Laboratory Practices (GLP) regulatory compliance. He has lectured throughout the world on these and other subjects. With an initial industry background in GLP Quality Assurance, Bill has a unique focus on quality improvements while improving efficiencies at the same time.
Whether a start-up, turnaround situation or simply, trying to be the best, VIDA Sciences can help. Increase market share, improve efficiencies and take quality to a new level. |
|
|
| |
Align yourself with successful experience from one of the world's largest preclinical CROs. From assessing your organizational structure, reviewing your quality systems or evaluating your performance effectiveness, VIDA Sciences has the experience to enable your success.
|
|
|
 Outsourcing through the continued and increased utilization of CROs is an integral part of bio-pharmaceutical strategies. VIDA Sciences assists small and medium sized biotechnology, medical device and pharmaceutical organizations navigate the outsourcing relationship and effectively manage them when selecting and utilizing CROs. |
|
Vivarium Operation Services |
|
You want your laboratory animal operation to achieve a higher level of success with improved animal welfare compliance, technical staff efficiency or becoming AAALAC accredited. Perhaps a client was unhappy with the performance of your laboratory animal operation, an outside inspection went poorly, or staff departures have caused setbacks. The decades of experience in vivarium operations at VIDA Sciences can elevate or resuscitate your animal laboratory.
|
|
|
|
GLP Regulatory Toxicology Expertise
VIDA Science's CEO Bill Harrison has vast knowledge of preclinical toxicology studies used to support INDs through NDAs. This experience will prove to be a great resource for any pharmaceutical, biotech or animal health organization worldwide.
Bill's experience includes assessing preclinical laboratories in North America, Europe, Japan, Australia and China.
From preplacement auditing, site selection, study monitoring, quality assessments, GLP compliance audits, ÿand alliance management, VIDA Sciences can facilitate communication and assure the quality of your regulatory research programs. Let us be an extension of your team!
Contact us today for a no obligation 30 minute consultation.
|
|
|
| |
|
