Experience. Excellence.
Founded in 1978, Lachman Consultants serves companies in Pharmaceutical, Medical Device/Combination Products, Biologics, and Regulatory Affairs. Each practice offers industry-leading experience and expertise in its area of focus.
Lachman Consultants serves emerging-to-enterprise organizations on a worldwide basis, delivering solutions that include FDA-Related Services, Audits & Mock Inspections, Quality Assurance & Controls, Scientific and Technical Assistance, Systems Evaluation, Regulatory Affairs, and Training, which consistently exceed client requirements and expectations.
When it comes to compliance and regulatory affairs, Lachman has set the industry standard through senior consultants, efficient engagements, integrated expertise, and loyal clients.
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51-200 employees
View all Lachman Consultant Services employees
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Pharmaceuticals
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1600 Stewart Ave., Suite 604, Westbury, NY NY11590, US
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1978
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Medical Devices, Regulatory, Training, Pharmaceuticals, Fda Compliance, Regulatory Affairs, Biologics, Cell Therapy, Anda, Nda, Gene Therapy, Expert Witness, Combination Products, Due Diligence Audits, Biologics, Generics, Facilities Validation, Drug Manufacturing, Fda-Related Services, Quality Assurance & Controls, Scientific & Technical Assistance, System & Process Validation, Warning Letter Remediation, 483 Response, Mock Pai, 483 Response, Compliance, Process Validation, Data Integrity, Audits, Quality Assurance, Training, Medical Dev
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Frances Marie Zipp is the CEO of Lachman Consultant Services.
The decision makers in Lachman Consultant Services are Charles Chuck Koon, Deanna Anderson, John Mcshane, etc. Click to Find Lachman Consultant Services decision makers emails.
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