Auditing- international - Import export

Qualification according to a list of criteria in order to evaluate the reliability of a company you have identified. Audit your manufacturers in China by sending an Asiaction inspector to the factory. Receive a full report of the visit.

The excellent knowledge of tax legislation and over 30 years of experience in the relations with government institutions and the tax administration in particular, allow us to plan and optimize your tax liabilities ultimately sparing your budget. We offer you: -Advice on direct and indirect taxation - ATINP, Act on Local Taxes and Fees /ALTF/, CITA, VAT Act, Act on Excise and Tax Warehouses /AETW/. -Tax protection at inspections – we render assistance during tax inspections, and this includes the preparation of written explanations, appeals and any other correspondence with the respective government institutions. -Protection against issued acts for administrative and tax violations – the difference at interpreting tax acts, regulations and their application sometimes leads to various administrative and tax penalties. In such cases we make statements, objections and comments to the parties. -Optimization of company tax liabilities and tax risk minimization, and overall tax planning.

Preparation of Statutory accounts for Sole Traders, Partnerships and Limited Companies.

CIC will be happy to support you in planning, securing, controlling, monitoring and optimizing your quality management, e.g. with: advanced quality planning supplier quality purchased part quality component qualification product engineering Supplier Audit Internal audits Process monitoring and process optimization Production control and monitoring at the supplier bottleneck coordination production readiness tool design Tool tracking mold trials Gauge concepts and gauge acceptance component measurements Resident Engineering Task Force Abbreviations such as APQP, PEP, FMEA, PPAP, 8-D, 5Why are not foreign words for us but common tools.

Our experienced team has for years done documentation for companies who are manufacturers of medical devices /surgical instruments. We provide Quality-Management-Systems for meeting legal and normative requirements. For manufacturers of medical devices / surgical instruments class I (including Is, Im, and new for MDR class Ir), IIa, and IIb we offer the following services:
 Implementation DIN EN ISO 13485 and the EU-Regulation 2017/745 MDR and 21 CFR 820 QSR Creating QM-Systems with procedural instructions and work instructions Technical Documentation Clinical evaluation Risk Management / Risk Analysis Essential Safety and Performance Requirements Validation of processes UDI-labeling Consulting for Regulatory Affairs Internal audits and external supplier audits Accompaniment and support with inspections by authorities and Audits by notified bodies Communication with authorities

LogBox is a log management solution in cloud that helps businesses manage collection, reporting, archiving and more. Perfect for SME business who need to be compliant to the GDPR law and need to do internal audit.