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藥包材相容性 Pharmaceutical packaging compatibility

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藥包材相容性研究是指考察與藥品直接接觸的包裝系統(tǒng)與藥物之間是否發(fā)生遷移或吸附的試驗過程。
對于吸入劑、注射劑、滴眼劑等高風(fēng)險制劑,需進(jìn)行藥包材相容性研究,以確保藥包裝系統(tǒng)的相容性與安全性。
產(chǎn)品詳情

1.我們服務(wù)的種類:

玻璃:鈉鈣輸液瓶;硼硅安瓿瓶、注射劑瓶;卡式瓶、預(yù)灌封注射器等;

塑料:輸液瓶、多層共擠輸液袋、滴眼劑瓶、藥用復(fù)合袋等;

橡膠:注射用溴/氯化丁基橡膠塞、覆膜膠塞;硅橡膠膠塞、墊片;預(yù)灌封、筆式注射器用溴/氯化丁基橡膠塞、墊片等;

2.我們研究的內(nèi)容:

1)可提取物研究(模擬研究)

2)浸出物研究

3)安全性評估

 3.我們研究的流程:

4.研究范圍(不僅限于):4. Research scope (not limited to) :

1.《藥品包裝材料與藥物相容性試驗指導(dǎo)原則》(YBB00142002-2015)

2.《化學(xué)藥品注射劑與塑料包裝材料相容性研究技術(shù)指導(dǎo)原則(試行)

3.《化學(xué)藥品與彈性體密封件相容性研究技術(shù)指導(dǎo)原則(試行)》

4.《化學(xué)藥品注射劑與藥用玻璃包裝容器相容性研究技術(shù)指導(dǎo)原則(試行)》

5.《中國藥典》2020年版

6.《ICH Q3C:Impurities:Guideline for Residual Solvents》

7.《ICH Q3D:Guideline For Elemental Impurities》

8.USP<232> Elemental Impurities

9.USP<381> Elastomeric closure for injection

10.USP<1663>Assessment of Extractables Associated with Pharmaceutical Packaging/Delivery System

11.USP<1664> Assessment of Drug Product Leachables Associated with Pharmaceutical Packaging/ Delivery System


1. Our service types:

Glass: sodium-calcium infusion bottle; Borosilicate ampoule bottle, injection bottle; Cassette bottles, pre-potting syringes, etc.;

Plastic: infusion bottle, multi-layer co-extruded infusion bag, eye drop bottle, pharmaceutical compound bag, etc.

Rubber: bromine/chlorinated butyl rubber plug for injection, coated rubber plug; Silicone rubber plug, gasket; Pre-potting, bromine/chlorinated butyl rubber plugs for pen syringes, gaskets, etc.;

2. What we study:

(1) Extractable Studies (simulation studies)

(2) Study on extracts

(3) Security assessment

3.Our research process:

①Information collection and evaluation

②Case study and design

③Extract study

④Extract data analysis, safety assessment

⑤Extractum method development

⑥methodology validation

⑦Extractum study

⑧Extractum data analysis, safety assessment

⑨Compatibility report

4. Research scope (not limited to) :

1.《藥品包裝材料與藥物相容性試驗指導(dǎo)原則》(YBB00142002-2015)

2.《化學(xué)藥品注射劑與塑料包裝材料相容性研究技術(shù)指導(dǎo)原則(試行)

3.《化學(xué)藥品與彈性體密封件相容性研究技術(shù)指導(dǎo)原則(試行)》

4.《化學(xué)藥品注射劑與藥用玻璃包裝容器相容性研究技術(shù)指導(dǎo)原則(試行)》

5.《中國藥典》2020年版

6.《ICH Q3C:Impurities:Guideline for Residual Solvents》

7.《ICH Q3D:Guideline For Elemental Impurities》

8.USP<232> Elemental Impurities

9.USP<381> Elastomeric closure for injection

10.USP<1663>Assessment of Extractables Associated with Pharmaceutical Packaging/Delivery System

11.USP<1664> Assessment of Drug Product Leachables Associated with Pharmaceutical Packaging/ Delivery System




藥包材相容性 Pharmaceutical packaging compatibility

藥包材相容性 Pharmaceutical packaging compatibility

分享到微信

×
藥包材相容性研究是指考察與藥品直接接觸的包裝系統(tǒng)與藥物之間是否發(fā)生遷移或吸附的試驗過程。
對于吸入劑、注射劑、滴眼劑等高風(fēng)險制劑,需進(jìn)行藥包材相容性研究,以確保藥包裝系統(tǒng)的相容性與安全性。
產(chǎn)品詳情

1.我們服務(wù)的種類:

玻璃:鈉鈣輸液瓶;硼硅安瓿瓶、注射劑瓶;卡式瓶、預(yù)灌封注射器等;

塑料:輸液瓶、多層共擠輸液袋、滴眼劑瓶、藥用復(fù)合袋等;

橡膠:注射用溴/氯化丁基橡膠塞、覆膜膠塞;硅橡膠膠塞、墊片;預(yù)灌封、筆式注射器用溴/氯化丁基橡膠塞、墊片等;

2.我們研究的內(nèi)容:

1)可提取物研究(模擬研究)

2)浸出物研究

3)安全性評估

 3.我們研究的流程:

4.研究范圍(不僅限于):4. Research scope (not limited to) :

1.《藥品包裝材料與藥物相容性試驗指導(dǎo)原則》(YBB00142002-2015)

2.《化學(xué)藥品注射劑與塑料包裝材料相容性研究技術(shù)指導(dǎo)原則(試行)

3.《化學(xué)藥品與彈性體密封件相容性研究技術(shù)指導(dǎo)原則(試行)》

4.《化學(xué)藥品注射劑與藥用玻璃包裝容器相容性研究技術(shù)指導(dǎo)原則(試行)》

5.《中國藥典》2020年版

6.《ICH Q3C:Impurities:Guideline for Residual Solvents》

7.《ICH Q3D:Guideline For Elemental Impurities》

8.USP<232> Elemental Impurities

9.USP<381> Elastomeric closure for injection

10.USP<1663>Assessment of Extractables Associated with Pharmaceutical Packaging/Delivery System

11.USP<1664> Assessment of Drug Product Leachables Associated with Pharmaceutical Packaging/ Delivery System


1. Our service types:

Glass: sodium-calcium infusion bottle; Borosilicate ampoule bottle, injection bottle; Cassette bottles, pre-potting syringes, etc.;

Plastic: infusion bottle, multi-layer co-extruded infusion bag, eye drop bottle, pharmaceutical compound bag, etc.

Rubber: bromine/chlorinated butyl rubber plug for injection, coated rubber plug; Silicone rubber plug, gasket; Pre-potting, bromine/chlorinated butyl rubber plugs for pen syringes, gaskets, etc.;

2. What we study:

(1) Extractable Studies (simulation studies)

(2) Study on extracts

(3) Security assessment

3.Our research process:

①Information collection and evaluation

②Case study and design

③Extract study

④Extract data analysis, safety assessment

⑤Extractum method development

⑥methodology validation

⑦Extractum study

⑧Extractum data analysis, safety assessment

⑨Compatibility report

4. Research scope (not limited to) :

1.《藥品包裝材料與藥物相容性試驗指導(dǎo)原則》(YBB00142002-2015)

2.《化學(xué)藥品注射劑與塑料包裝材料相容性研究技術(shù)指導(dǎo)原則(試行)

3.《化學(xué)藥品與彈性體密封件相容性研究技術(shù)指導(dǎo)原則(試行)》

4.《化學(xué)藥品注射劑與藥用玻璃包裝容器相容性研究技術(shù)指導(dǎo)原則(試行)》

5.《中國藥典》2020年版

6.《ICH Q3C:Impurities:Guideline for Residual Solvents》

7.《ICH Q3D:Guideline For Elemental Impurities》

8.USP<232> Elemental Impurities

9.USP<381> Elastomeric closure for injection

10.USP<1663>Assessment of Extractables Associated with Pharmaceutical Packaging/Delivery System

11.USP<1664> Assessment of Drug Product Leachables Associated with Pharmaceutical Packaging/ Delivery System




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