FACILITIES & MANUFACTURING

ASSURING THE HIGHER QUALITY SANDARDS FOR SAFETY AND EFFICIENCY OF MANUFACTURING

*STRINGENT REGULATORY REQUIREMENTS FOR EXTRA SAFETY

TESSLIFT FACILITY HAS ISO 13485 TUV SUD CERTIFICATION AND OTHER INTERNATIONAL GMP STANDARDS. WE HEAVILY FOCUS ON MANUFACTURING SOLUTIONS TO MEET STRINGENT REGULATORY REQUIREMENTS. OUR CLEANROOMS ARE DESIGNED AND MANAGED BY THE REGULATORY AND QUALITY EXPERTS FOR MEDICAL DEVICES. FURTHERMORE, WE ARE ENGAGED WITH CGMP AND FDA STRATEGIC PARTNERS FOR RAW MATERIALS.

*AUDITING PROGRAMS AND REGULAR TRAININGS

ALL FINISHED PRODUCTS ARE VERIFIED FOR THEIR PERFORMANCE, SAFETY, AND QUALITY. THROUGHOUT THE YEAR, TESSLIFT UNDERGOES VARIOUS AUDITING PROGRAMS TO ENSURE AND MEET ALL FACILITIES/MANUFACTURING STANDARDS WITH THE MOST UPDATED VERSIONS. ALL EMPLOYEES RECEIVE REGULAR TRAINING TO HELP THEM USE THE FACILITIES TO THEIR MOST EFFICIENT LEVEL.

INTEGRATIVE AUDITING PROGRAM

CLEANROOM

QUALITY MANAGERS ATTEND INTERNATIONAL CONFERENCES

QUALITY TEAM MEMBERS OBTAIN REGULAR TRAININGS LOCALLY

ALL EMPLOYEES ARE RECOGNIZANT OF THE MOST UPDATED VERSION OF STANDARS FOR EACH FACILITY UNIT

R&D CENTER / MANUFACTURING

GLOBAL PROJECTS FOCUSING ON EXTENSIVE CLINICAL SAFETY AND ADEQUATE MARKET STRATEGIES.

THE WORLD LEADER IN SOFT TISSUE APPROXIMATION TECHNOLOGY.

QUALITY MANUFACTURING IN ACCORDANCE WITH THE STRINGENT STANDARDS.

COLLABORATIVE PROJECTS AND GOVERNMENT FUNDED PROJECTS ARE IMPORTANT ASSETS TO OUR R&D PROGRESS

TESSLIFT’S GOVERNMENT LICENSED R&D CENTER MAKES THE CONTINUOUS PROGRESS.

TESSLIFT’S PRODUCTS ASSURED BY THE COMPREHENSIVE AUDITING MANAGEMENT.

OUR BRANDS

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