EXPERIENCE. EXCELLENCE.
PHARMACEUTICAL
Lachman Consultants has an unsurpassed reputation for excellence in technical, regulatory consulting, and guidance services for the Pharmaceutical Industry, including generic and new drug products, OTC, and monograph drugs, and many more.
Lachman Consultants excel in the development, implementation, and management of diversified projects involving compliance, scientific principles, technical aspects, and regulatory requirements related to pharmaceutical products.
SCHEDULE A CONSULTATION MEET LEADERSHIP TEAM
FDA & EMA Compliance
- Compliance Enhancement Plans
- GxP Audits
- Quality Systems Remediation
- SOP Development & Review
- Due Diligence Audits
- Training
- Batch Record Reviews
- Protocol Development and Reviews
- Compliance Problem Resolution
Data Governance & Integrity
- Assessments of maturity and gaps
- Custom-fit program design and consulting
- Phased, risk-based implementation planning
- End-to-end construction and delivery including:
- Forensic analysis of data
- Detailed data integrity vulnerability / risk assessments of systems
and processes - Integration of data governance throughout QMS
- Training for all levels from shop floor to executives
- Periodic health checks to ensure your program remains sustainable,
contemporary, and effective
ADVANCE CONFIDENTLY
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