Qingdao Running Machine Co.,Ltd quality control

China Qingdao Running Machine Co.,Ltd certification
China Qingdao Running Machine Co.,Ltd certification
Customer Reviews
I am site manager of iron mining company in Australia; We used to pay large amount for rent conveyor belt splice tool from local supplier; Mac provide another solvtion for us, they vulcanizer are cheap and good to use, the price is nearly as much as the rent fee for one year, We can save a lots of budget; —— Mr Jack

—— Jack

I have purchased conveyor belt vulcanizing machine from Qingdao running machine company through their representative Miss lily. I must say machine is running perfectly and very smooth in very good competitive price and their company behaviour is so cooperative. After sale service is so perfect that I never hesitate to ask any questions after buying

—— Junaid Ali

Package was sturdy and contained everything without damage. Parts of machines are so well equipped with new technology. I always pray for Mr. Mike that him and his company will achieve best milestones in term of quality and their services.

—— Jay Crue

Recommended 100% Good value for the money!

—— Richard S.

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QC Profile

Products manufactured in the LCGM adhere to the following GMP/Quality Attributes:

Qingdao Running Machine Co.,Ltd quality control 0


Products for phase I investigations are developed as outlined in the FDA Guidance for Industry: INDs — Approaches to Complying with CGMP During Phase 1 and products for use in Phase II studies will be manufactured according to the requirements of Good Manufacturing Practice (21CFR 210, 211, 1271)

All activities are performed per Quality Assurance approved documents. Good documentation practice ensures compliance with GMP requirements.

Only qualified personnel perform the manufacturing, testing and release of products.

Starting materials are selected, verified to be obtained from appropriate supplier; certificate of analysis (testing) evaluated; materials inspected and dispositioned (release, reject and quarantine) prior to use.

Equipment is installed and maintained as per manufacturer’s requirements. Critical process equipment is maintained and calibrated to ensure functionality remains appropriate for intended purpose. All refrigeration and cell culture equipment used in manufacturing and testing is monitored by REES, qualified electronic monitoring system.

Effective environmental monitoring (eg. personnel, in process, non-viable, surface) and control systems are implemented to maintain a state of control to achieve product quality.

Segregation of materials, documents, products, samples and equipment is maintained to prevent cross contamination.

Samples and products are handled, stored and distributed in a manner that ensures quality is maintained throughout the sample or product life cycle.

Specification for analytical methods are approved by QC based on empirical evidence.

When performing product lot disposition, a review of manufacturing and analytical execution, adherence to procedure and in process controls are evaluated prior to product release.

Root cause analysis is employed as required during investigations of deviations and quality/product issues with intent to implement corrective actions designed to prevent reoccurrence. The appropriate determination of cause enables the identification of Corrective Action/Preventive Action (CAPA) with their implementation being monitored for effectiveness.

Products are released after QA has evaluated and approved the product to have been produced within established process and release requirements.

GMP outsourced activities are managed through quality agreements between LCGM and contract testing site. The Quality Agreement describes the requirements the contract testing site must comply with to maintain quality of product.

Proposed changes are evaluated through Change Control where the change is assessed for any regulatory/GMP/product impact and approved prior to implementation.

An independent audit is periodically conducted to ascertain the effectiveness of the Quality Systems Program.

Periodic management review of the Quality Systems is required to understand effectiveness and potential improvements of processes and systems.

Qingdao Running Machine Co.,Ltd quality control 1

Materials are manufactured for pre-clinical safety studies as outlined in the FDA Guidance for Industry: Preclinical Assessment of Investigational Cellular and Gene Therapy Products (November 2013)

  • China Qingdao Running Machine Co.,Ltd certification

    Standard:Certificate of Conformity


    Issue Date:2013-03-16

    Issued By:国家防爆电气产品质量监督检验中心

  • China Qingdao Running Machine Co.,Ltd certification

    Standard:Safety mark certificate


    Issue Date:2021-02-03

    Expiry Date:2026-02-02

    Issued By:安标国家矿用产品安全标志中心有限公司

  • China Qingdao Running Machine Co.,Ltd certification

    Standard:Certificate of Conformity


    Issue Date:2021-06-22

    Expiry Date:2026-05-11

    Issued By:国家安全生产上海矿用设备检测检验中心

  • China Qingdao Running Machine Co.,Ltd certification



    Issue Date:2018-01-05

    Expiry Date:2023-01-04

  • China Qingdao Running Machine Co.,Ltd certification



    Issue Date:2017-01-21

    Issued By:SGS

Contact Details
Qingdao Running Machine Co.,Ltd

Contact Person: Miss. Lily Fu

Tel: +86 130 6133 2206

Fax: 86-532-8719-2258

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