2004年12月16日 · OTS = Off Tooling Sample Put it simply: The piece which your customer will continue to receive in future during serial production, what means "you see is what you get". Different from prototype. Prototype is still open for changes. That's why OTS follows what the PPAP defines as the final piece of sample. some day to day example of OTS:

2010年8月20日 · In OTS approve step, OTS sample is approved by development Dept. now. Many times, measurement,function ,material or DVP test rusult is nonconforming,or DVP test item is not complete.But project time is urgent, so development Dept. approve the OTS sample,also release the report and SQE do not know.

2005年7月17日 · Welcome to the cove This is the definition that I have PVS=Pre-production run The Pre-production run is used for fine tuning of the production and assembly processes of the individual parts.

Phased Production Part Approval Process Phased PPAP Requirements Handbook Ford Motor Company Supplier Technical Assistance

2010年6月6日 · Dear Frinds some one ask me question to forward to you. If we are purchase our material from the local market like shops and retail markets, so when we need a material the purchasing man go their with our requirements and get the material with cheapest price and good quality so we can...

2018年7月10日 · My opinion is that GAMP is too much for most of the medical device industry. ISO TR 80002-2 was created to specifically deal with the new "risk based" activities of ISO 13485:2016, meaning you can tailor the process depending on the risk. There's several other guidances, general and for other industries.

2013年9月7日 · I would like to have a clear definition for each phase of these four stages( VFA PVS 0-Series S-Series) of a VW Program. If You have some experience with VW. And Wich Phase a PPAP should be sent in general to the Customer? I mean a staged PPAP one for each Phase or just in one precise stage.

2011年3月30日 · Re: Injection moulding - definitions of T0, T1 samples No, T0, T1, T2 are recognised terms when supplying the first off-the-tool sample plastic parts to a customer for evaluation.

2013年1月31日 · Re: Validation of OTS software in medical device There is a subtlety on this subject. OTS encapsulated into the device needs to be validated to ensure the safety of the device, whereas OTS used to create/etc. the device needs to be validated to comply with 21CFR820.70(i), and OTS relates to verification should be because of 21CFR820.72(a).

2008年1月5日 · I am confused that which sample can be introduced for PV test or DV test, we are one Automotive company, during our localization period, our ENG guy ask all raw material should be release ( that means catch drawing ) for their DV test …