
Acro
Pharmaceuticals, 601 Ave Nw Ste 350, Washington, District of Columbia, New Jersey, 20001, United States, 1-10 Employees
Phone Number: 20********
Who is ACRO
ACRO advocates as the collective voice of innovative clinical research and technology organizations to regulators and policymakers, educating stakeholders and shaping policies that foster...
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Headquarters: 601 New Jersey Ave Nw Ste 350, Washington, District of Columbia, 20001, United States
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Date Founded: 2002
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Employees: 1-10
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Revenue: $1 Million to $5 Million
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Active Tech Stack: See technologies
Industry: Pharmaceuticals
SIC Code: 8611
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NAICS Code: 813910 |
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ACRO Org Chart and Mapping
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Frequently Asked Questions Regarding ACRO
Answer: ACRO's headquarters are located at 601 Ave Nw Ste 350, Washington, District of Columbia, New Jersey, 20001, United States
Answer: ACRO's phone number is 20********
Answer: ACRO's official website is https://acrohealth.org
Answer: ACRO's revenue is $1 Million to $5 Million
Answer: ACRO's SIC: 8611
Answer: ACRO's NAICS: 813910
Answer: ACRO has 1-10 employees
Answer: ACRO is in Pharmaceuticals
Answer: ACRO contact info: Phone number: 20******** Website: https://acrohealth.org
Answer: ACRO advocates as the collective voice of innovative clinical research and technology organizations to regulators and policymakers, educating stakeholders and shaping policies that foster efficient, effective, and safe conduct of clinical research. Since our founding in 2002, ACRO has been committed to strengthening public understanding and confidence in clinical research. ACROs membership has evolved from being comprised entirely of global CROs to now including several of the industrys technology partners. ACRO looks to demonstrate the important contribution that CROs and technology companies make as partners in the development of new medicines and new treatments. The association is a leading voice for safe and ethical clinical trials, working with stakeholders globally to explore new paradigms for research and development and to promote a more innovative, safe, and efficient clinical trial process. As an association, we are especially interested in areas such as the expansion of the adoption of DCTs, RBQM, diversity and inclusion in clinical trials, enhancing the efficiency of R&D, data sharing, data protection and privacy, technology innovation, real-world evidence, patient-centered drug development, safety and ethics in clinical research, tax policies that support research and innovation, and a host of global regulatory issues.
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