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hydraulic cylinder parts breakdown

Established in 2001, Puyang Zhong Yuan Restar Petroleum Equipment Co.,Ltd, “RSD” for short, is Henan’s high-tech enterprise with intellectual property advantages and independent legal person qualification. With registered capital of RMB 50 million, the Company has two subsidiaries-Henan Restar Separation Equipment Technology Co., Ltd We are mainly specialized in R&D, production and service of various intelligent separation and control systems in oil&gas drilling,engineering environmental protection and mining industries.We always take the lead in Chinese market shares of drilling fluid shale shaker for many years. Our products have been exported more than 20 countries and always extensively praised by customers. We are Class I network supplier of Sinopec,CNPC and CNOOC and registered supplier of ONGC, OIL India,KOC. High quality and international standard products make us gain many Large-scale drilling fluids recycling systems for Saudi Aramco and Gazprom projects.

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hydraulic cylinder parts breakdown
Possible Causes of Out of Specification : Pharmaceutical ...
Possible Causes of Out of Specification : Pharmaceutical ...

Possible Causes of Out of Specification 1. Test Analysis Error in QC Lab: Error in the QC lab is human or analyst error. This is the most probable cause of the... 2. Lab Equipment Malfunctioning: Due to this problem analysis is also unaware of the occurrence of this error. Sometimes... 3. Production ...

Out Of Specification Investigations.
Out Of Specification Investigations.

OOS / OOT/ Atypical Result • ,Out,-of-,Specification, (OOS) Result – test result that does not comply with the pre-determined acceptance criteria (i.e. for example, filed applications, drug master files, approved marketing submissions, or official compendia or internal acceptance criteria).

Out Of Specification Investigations.
Out Of Specification Investigations.

OOS / OOT/ Atypical Result • Out-of-Specification (OOS) Result – test result that does not comply with the pre-determined acceptance criteria (i.e. for example, filed applications, drug master files, approved marketing submissions, or official compendia or internal acceptance criteria).

Management of Out of Specification (OOS) for Finished Product
Management of Out of Specification (OOS) for Finished Product

In pharmaceutical industry, out-of-specification (OOS) test results are results that (after rounding off) fall outside the specifications of established acceptance criteria.

Manual 058 Out of Specification Results Investigation
Manual 058 Out of Specification Results Investigation

3.1 Out of Specification (OOS) Test Result A laboratory test that is outside its regulatory or compendial limits. In some cases, there may be additional tests and/or limits that are used to assess the quality of a material, but are not included in registrations or compendia. In these cases, the

Out of Specification Software | OOS Software | MasterControl
Out of Specification Software | OOS Software | MasterControl

Out of Specification (OOS) The out-of-specification (OOS) product in the MasterControl Quality Management System (QMS) allows for seamless compliance. Interconnected OOS software lets you …

How to investigate Out of Specification (OOS) Laboratory ...
How to investigate Out of Specification (OOS) Laboratory ...

15/1/2015, · What is out of specification result? Out of specification implies test results which fall outside specifications or acceptance criteria established by the product manufacturer or the laboratory. Investigation of out of specification results. Out of specification results can result from either of the two situations. Laboratory testing errors. Or

FDA Guidelines-For Out of Specifications (OOS) – Chemistry ...
FDA Guidelines-For Out of Specifications (OOS) – Chemistry ...

7/12/2020, · If the ,OOS, is confirmed the batch is rejected and if the ,OOS, is found inconclusive then QA may be able to justify and release the batch. Key words: cGMP regulations, ,OOS,, Quality control unit, Batch rejection. INTRODUCTION: It provides agency’s current thinking on ,out of specification, …

Guidance for Industry
Guidance for Industry

Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production, . This guidance, represents, the, Food and Drug Administration's (FDA's) current thinking, on this topic. It

SOP for Out of Specification (OOS) for Pharmaceutical ...
SOP for Out of Specification (OOS) for Pharmaceutical ...

SOP for Out of Specification (OOS) for Pharmaceutical Results Standard operating procedure to handle the out of specification results during the analysis of Pharmaceutical products and its investigation report during different stages.

Insights on OOS Investigation Guidelines and Compliance
Insights on OOS Investigation Guidelines and Compliance

The official definition of OOS is “A specification (often abbreviated as ‘spec’) is an explicit set of requirements to be satisfied by a material, product, or service. Should a material, product, or service fail to meet one or more of the applicable specifications, it is referred to as being out of specification.”.

Out of Specification Guidance - MHRA Inspectorate
Out of Specification Guidance - MHRA Inspectorate

The issue faced when dealing with out of specification (OOS) results is as much a challenge now as it ever was. Without doubt the most common deficiency raised, is the one where the OOS result has...

Out of specification (oos)1 - SlideShare
Out of specification (oos)1 - SlideShare

13/11/2014, · Out of specification (oos)1 1. Dr Ravi Kinhikar Handling OOS (Out of Specification) 2. What is Out of Specification (OOS) The result obtained out of defined test limit is called out of specification. 3. History Of OOS guideline Event Year USFDA audited Barr Laboratory, identified attempt of “Test ...

Out of Specification (OOS) and Out of Trend (OOT)
Out of Specification (OOS) and Out of Trend (OOT)

Out of specification (OOS) is defined as a result that falls outside the predetermined specifications or established acceptance criteria set by the manufacturer and/or the laboratory. In simple terms, the result of a stability test conducted by a Quality Analyst (QA) should always adhere to the previously established specifications or criteria.

SOP on Handling of Out of Specification Results in quality ...
SOP on Handling of Out of Specification Results in quality ...

When an Out-Of-Specification test result is generated/ suspected, the analyst shall inform to the QA Manager immediately about the test results. OOS number shall be allocated in the following manner. OOS/YY/XXX, where OOS represent the Out of specification, YY indicates the last two digits of the year & XXX indicates the serial number from 001 to 999.

GMP-OOS - Accepting the GMP Out-of-Specification Test Results
GMP-OOS - Accepting the GMP Out-of-Specification Test Results

The term Out-of-specification is used so often in pharmaceutical industry, but many of us are still unaware of its meaning. Well, when a drug undergoes stability testing or release testing and the tests results aren’t within the limits of pre-defined specifications, it is said to be Out-of-Specification result that may trigger an OOS investigation.

Out of Specification Handling a OOS - Pharma Engineering
Out of Specification Handling a OOS - Pharma Engineering

5.3.1 Out of specification (OOS) results in the bacteriological testing may be due to high total bacterial count and total fungal count or due to presence of any specified organism in the sample.

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