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Sectors
Pharmaceutical and Biotech
Products
ManVa. Validation of SaaS systems
CalCroma. Automation of chromatographic systems
TraceDesk. Serialisation and Traceability Solutions
Digital Validation
Praas. Periodic reviews of computer systems
Consultancy services
Validation of IT systems
Cualificación de equipos e instalaciones
Audit and consultancy GMP, GCP, GLP, GDP and GVP
Data Integrity
Medical Devices
Products
eQMS. Electronic Quality Management System
RaaSDesk. Periodic reviews of computer systems
ARI. Automated Regulatory Intelligence
Templates for quality and regulatory affairs management
AReIA. Transform your Regulatory Affairs department
Consultancy services
Gap Analysis
Internal audit
Due Diligence
Regulatory and Clinical Strategy
Digital Solutions
Products
Automated sellout app for the veterinary pharmaceutical industry
Consultancy services
ITSM & ITOM Solutions
IAM: Identity and Access Management
Global device management and security
IT systems qualification
Areas
Validation and qualification
ManVa: Validation of SaaS systems
Digital Validation
Validation of IT systems
Qualification of equipment and installations
IT systems qualification
Audits
Gap Analysis
Internal audit
Due Diligence
Regulation and Quality (RA/QA)
Regulatory Affairs Management
ARI. Automated Regulatory Intelligence
AReIA. Transform your Regulatory Affairs department
Regulatory and Clinical Strategy
Audit and consultancy GMP, GCP, GLP, GDP and GVP
Data Integrity
Praas. Periodic reviews of computer systems
eQMS. Electronic Quality Management System
Digital Transformation
TraceDesk. Serialisation and Traceability Solutions
CalCroma. Automation of chromatographic systems
Automated sellout app for the veterinary pharmaceutical industry
ITSM & ITOM Solutions
IAM: Identity and Access Management
Global device management and security
Talent
Outsourcing
Headhunting
Work with us
Training
Online and customised training
Information Systems
Implementation of Automatic Calculations in Chromatographic Systems
IT Quality System in a regulated environment
Evaluation of suppliers in IT environments
Validation of IT systems
IT Systems in Regulated Industry - Overview
Maintenance of validation status in IT systems
Periodic review of computer systems
GMP's
GMP documentation management
Good Manufacturing Practice (GMP): Equipment Qualifications
Medical Devices
Quality Management System for medical devices according to ISO 13485
Risk management for medical devices according to ISO 14971
Medical Software Validation
Data Integrity
Data Integrity - Global Vision
Resources
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Contenidos especializados
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