Training Services
Core Advantages
Six major curriculum systems provide comprehensive coverage, spanning from operation to validation, and from maintenance to regulatory compliance.
01
Sterilization Validation Training
EO sterilization process validation, sterilization qualification, microbial challenge testing, residue verification, preparation of validation documentation, and deviation management.
Suitable for:
Quality Manager
Verification Engineer
Registration Officer
02
Sterilization Procedure Training
Standard operating procedures for sterilization equipment, loading protocols, parameter monitoring, anomaly handling, daily record-keeping, and aseptic technique guidelines.
Suitable for:
Workshop Sterilization Supervisor
Workshop Sterilization Operator
Production Team Leader
03
Sterilization Equipment Maintenance and Service Training
Daily inspections, periodic maintenance, troubleshooting, component replacement, equipment calibration, and establishment of maintenance records for sterilizers.
Suitable for:
Workshop Equipment Manager
Equipment Engineer
Mechanical Maintenance Technician
04
Regulatory and Standards Training
Interpretation of Updates to National Sterilization Standards, ISO 11135, ISO 13485, the New Regulations on Medical Device Sterilization, and Domestic and International Sterilization Laws and Regulations
Suitable for:
Quality Manager
Compliance Officer
System Specialist
05
Quality System Training
Sterile product quality control, risk assessment, batch record management, nonconforming product control, internal audit procedures, and continuous improvement.
Suitable for:
Quality Manager
QA/QC
Internal auditor
06
GMP Training Guidelines
Implementation of GMP sterility requirements for pharmaceuticals and medical devices, on-site workshop rectification, GMP audit preparation support, establishment of a document management system, and mock audits.
Suitable for:
Enterprise principal
Quality Manager
Production Manager
Core Advantages
Five core training advantages
Drafting unit of the industry standard
With a team of dozens of seasoned instructors and as a drafting body for industry standards, we possess an in-depth understanding of numerous standards, identify our clients’ key knowledge gaps, and, in alignment with applicable regulations, deliver tailored solutions.
Real-World Operational Training
We operate our own on-site sterilization service centers, routinely handling batch‑scale product sterilization. Our training is grounded in real‑world mass‑production sterilization scenarios, enabling trainees to tackle authentic production challenges, with hands‑on exercises that can be directly implemented in enterprise workshops.
End-to-end hands-on training
The training facility is equipped with sterilizers, pre-processing and decontamination systems, exhaust-gas treatment units, automated transfer equipment, and more. Hands-on, group-based exercises are conducted, moving beyond mere observation to provide comprehensive, practical experience across the entire workflow—from loading and operation to testing and maintenance.
A training certificate will be issued upon successful completion of the assessment.
Upon completion of the training, candidates will undergo both theoretical and practical assessments. Upon passing, they will receive an official manufacturer‑issued training certificate and a sterilization‑operation certification for authorized personnel. These certificates are recognized for internal employment purposes, GMP audits, and inspections, and may be filed for record‑keeping.
Training Scenario
Realistic Training Base
R&D Training Base
Sterilization Equipment Training Workshop
Sterilization Equipment Training Workshop
Customer Reviews
Customer Reviews
”
I attended a validation engineer training course, where the instructor started with the device’s underlying logic, giving me a completely new understanding of EO sterilization validation. Upon returning, I independently completed the preparation of the validation protocol.
A certain sterile pharmaceutical enterprise
Verification Engineer
”
In-house corporate training is highly practical. The instructor took the time to familiarize themselves with our equipment and product lines, and the customized curriculum precisely addressed our key pain points. Highly recommended.
A certain medical device company
Production Director
”
The manufacturer’s training is highly practical; after employees obtain their certification, the workshop’s sterilization procedures have been significantly standardized, enabling smooth passage of the GMP inspection.
A medical consumables company
Quality Director
Baijiahao
TikTok
WeChat Official Account
Email: rongfeng@88.com
Address: No. 5, Chicheng West, Zhongjie Medical Device Park, Cangzhou City, Hebei Province