Welcome to the company ! we have many years of professional experience !
rsdgj@pyzyrsd.com +86 13525609655

tap drill sizes chart

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.

Certificate of Honor

CONTACT US

Customer satisfaction is our first goal!

Phone

+86 13525609655

E-Mail

rsdgj@pyzyrsd.com

Address

Road West, North Branch, Jingkai Road, Puyang City

tap drill sizes chart
Gravimetric Sample Preparation - out of specification errors
Gravimetric Sample Preparation - out of specification errors

Out,-,of-Specification, (,OOS,) investigations in analytical R&D and QA/QC laboratories are costly and time-consuming. Download the White Paper . Science Based Weighing Standard for …

(PDF) Out of specification (OOS) and Out of Trend (OOT ...
(PDF) Out of specification (OOS) and Out of Trend (OOT ...

PDF | On Dec 15, 2018, Sagar Savale published ,Out of specification, (,OOS,) and ,Out, of Trend (OOT) ,analysis in Pharmaceutical Manufacturing Investigations (MIR): A, Overview | Find, read and cite all ...

OOS Investigation Tools & Software Out of Specification ...
OOS Investigation Tools & Software Out of Specification ...

Investigating ,Out of Specification, (,OOS,) lab results is a necessity for every pharmaceutical and combination product manufacturer. Both cGMP and 21 CFR part 210 and 211 requirements guide the process for investigating ,OOS, lab results for drug components, APIs, and finished drugs.

Out-of-Specification (OOS) | Atypical Laboratory Results ...
Out-of-Specification (OOS) | Atypical Laboratory Results ...

Attend this seminar to learn various terms used by regulators associated with investigations of atypical or ,out of specification, results (,OOS,), and how to document those investigations. Seminar will cover FDA Guidance, ,OOS, test results for pharmaceutical production and lab situations. You will also learn to create laboratory investigation checklist, documentation and CAPA.

INVESTIGATING OUT OF SPECIFICATION (OOS) TEST RESULTS …
INVESTIGATING OUT OF SPECIFICATION (OOS) TEST RESULTS …

IDENTIFYING AND ASSESSING ,OOS, TEST RESULTS:- FDA regulations require that an investigation be conducted whenever an ,OOS, test result is obtained.The purpose of the investigation is to determine the cause of the ,OOS,. Even if a batch is rejected based on an ,OOS, result, the investigation is necessary to determine if the result is associated with other batches of the same drug product or other ...

(PDF) Out of specification (OOS) and Out of Trend (OOT ...
(PDF) Out of specification (OOS) and Out of Trend (OOT ...

PDF | On Dec 15, 2018, Sagar Savale published ,Out of specification, (,OOS,) and ,Out, of Trend (OOT) ,analysis in Pharmaceutical Manufacturing Investigations (MIR): A, Overview | …

Out of Specification Guidance - Update by MHRA - PharmaLex
Out of Specification Guidance - Update by MHRA - PharmaLex

The MHRA first published guidance to industry on how to handle ,Out Of Specification, (,OOS,) investigations in August 2013. It has recently been reviewed and improved for ease of use. When this guidance was released in 2013, it saw a shift in how ,OOS, investigation were to be handled.

How to Handle Out of Specification (OOS) Results
How to Handle Out of Specification (OOS) Results

You receive a call late one night that your cold room went down and is now operating at ambient room temperature. Given the increase in temperature, the batch of drug product that was residing in that cold room is now questionable – in the pharmaceutical industry, we refer to this product as ,Out of Specification, (,OOS,).

Gravimetric Sample Preparation - out of specification errors
Gravimetric Sample Preparation - out of specification errors

Out,-,of-Specification, (,OOS,) investigations in analytical R&D and QA/QC laboratories are costly and time-consuming. Download the White Paper . Science Based Weighing Standard for …

FDA Guidelines-For Out of Specifications (OOS) In Industries
FDA Guidelines-For Out of Specifications (OOS) In Industries

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, and test results. Purpose of this document is

Laboratory Controls Overview and OOS / OOT Handling ...
Laboratory Controls Overview and OOS / OOT Handling ...

As such, GMP inspectors are looking into how companies manage ,OOS, results and one of the objectives of this course is to help you understand the current best practices for ,OOS, investigations. This 1-day course will step you through the key elements and basic principles for sustaining compliance in QC laboratories, with specific focus on ,OOS, Handling.

STANDARD OPERATING PROCEDURE FOR HANDLING OF OUT OF ...
STANDARD OPERATING PROCEDURE FOR HANDLING OF OUT OF ...

5.6 The analyst must report the ,OOS, results to Report Head / Study Director as soon as possible (within 24 hours), so that the laboratory investigation is performed timely. 5.7 Numbering of ,Out Of Specification,(,OOS,) 5.7.1 All ,Out Of Specification, shall be numbered as per unique numbering system of 14 characters as below: ,OOS,/XXX/YY/ZZZ

Guide to Out of Specification Analytical Results
Guide to Out of Specification Analytical Results

though it is useful to be aware of the slight differences (these are pointed ,out, in this guidance document where applicable). The FDA guide is entitled “Guidance for Industry Investigating ,Out,-of-Specification (,OOS,) Test Results for Pharmaceutical Production – October 2006” and is …

FDA Guidelines-For Out of Specifications (OOS) In Industries
FDA Guidelines-For Out of Specifications (OOS) In Industries

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, …

Questions and answers on the use of out-of-specification ...
Questions and answers on the use of out-of-specification ...

Questions and answers on the use ,of out-of-specification batches, of authorised cell/tissue-based advanced therapy medicinal products. 1. What is the pathway for the exceptional administration of ,out,-,of-specification, (,OOS,) batches of a cell/tissue based advanced therapy medicinal products (ATMPs) that have been granted a marketing authorisation?

[OOS] Q & A - Session 1 - Pharmaprinciple
[OOS] Q & A - Session 1 - Pharmaprinciple

Spread the Knowledge In this section i have quoted ten questions and related answers on the topic ,Out of specification, (,OOS, ) which will enrich the general knowledge for the pharma professionals. Let us find the Answers. Q1: In which section of 21 CFR 211 it is written that, it need to conduct an investigation if […]

Out of Specification definition - Law Insider
Out of Specification definition - Law Insider

Any ,Out, of Trend or ,Out of Specification, data should be addressed and subject to investigation. You acknowledged that your analysts failed to document and start investigating ,OOS, results, as required by your SOP 01-045/03 “Handling of Incidents” and SOP 08-004/12 “Laboratory Investigation of ,Out of Specification, Results.”

Chat Online Inquiry Email

Business cooperation

+86 13525609655

Company address

Road West, North Branch, Jingkai Road, Puyang City