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Pictures of medical staff protective masks

Shanghai Sunland Industrial Co., Ltd is the top manufacturer of Personal Protect Equipment in China, with 20 years’experience. We are the Chinese government appointed manufacturer for government power,personal protection equipment , medical instruments,construction industry, etc. All the products get the CE, ANSI and related Industry Certificates. All our safety helmets use the top-quality raw material without any recycling material.

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Solutions to meet different needs

We provide exclusive customization of the products logo, using advanced printing technology and technology, not suitable for fading, solid and firm, scratch-proof and anti-smashing, and suitable for various scenes such as construction, mining, warehouse, inspection, etc. Our goal is to satisfy your needs. Demand, do your best.

Highly specialized team and products

Professional team work and production line which can make nice quality in short time.

We trade with an open mind

We abide by the privacy policy and human rights, follow the business order, do our utmost to provide you with a fair and secure trading environment, and look forward to your customers coming to cooperate with us, openly mind and trade with customers, promote common development, and work together for a win-win situation.

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The professional team provides 24 * 7 after-sales service for you, which can help you solve any problems

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Consultation hotline:0086-15900663312

Address:No. 3888, Hutai Road, Baoshan District, Shanghai, China

Pictures of medical staff protective masks
Clinical Trial Solutions - IQVIA
Clinical Trial Solutions - IQVIA

Personalized medicine offers tremendous hope for patients. This change in focus to specialty treatments for highly defined patient populations also requires a change in how ,research, works, customized just as specifically as the treatments it is designed to test.

Development & Approval Process | Drugs | FDA
Development & Approval Process | Drugs | FDA

The main consumer watchdog in this system is FDA's Center for Drug Evaluation and ,Research, (CDER). The center's best-known job is to evaluate new drugs before they can be sold.

ANNEX 1 WHO GUIDELINES ON CLINICAL EVALUATION OF …
ANNEX 1 WHO GUIDELINES ON CLINICAL EVALUATION OF …

research, data include details of the ,development, and production of a vaccine together with reports of control ,testing,, which should be adequate to justify subsequent ,clinical, studies in humans. Phases ,of clinical development, (I-III) ,Clinical, trials in humans are classified into three phases: phase I, phase II and phase III. In certain countries ...

Clinical Trial Solutions - IQVIA
Clinical Trial Solutions - IQVIA

Personalized medicine offers tremendous hope for patients. This change in focus to specialty treatments for highly defined patient populations also requires a change in how ,research, works, customized just as specifically as the treatments it is designed to test.

R&D Systems: Products & Services for Cell Biology Research
R&D Systems: Products & Services for Cell Biology Research

R&D Systems is a global resource for cell biology. Find quality proteins, antibodies, ELISA ,kits,, laboratory reagents, and tools.

PAR-19-253: Focused Technology Research and Development ...
PAR-19-253: Focused Technology Research and Development ...

Early stage technology ,development, can be described in two stages: (I) exploratory proof-of-concept ,research, to determine the best approach(es) for a technology ,development, project, and (II) the subsequent ,research and development, that focuses exclusively on creating and validating a working prototype technology before ,application, to untested biomedical problems is possible.

Phases of Drug Development Process Drug Discovery Process ...
Phases of Drug Development Process Drug Discovery Process ...

The complexity in drug ,development, has increased manifolds over the past 40 years, requiring preclinical ,testing,, investigational new drug (IND) ,applications,, and completed ,clinical testing, before marketing approval from the FDA. Generally, new drug ,applications, (NDAs) or biologics license ,applications, (BLA) are reviewed comprehensively before approval, and then drug performance is resubmitted ...

SARS-CoV-2 Detection & Research Solutions
SARS-CoV-2 Detection & Research Solutions

PerkinElmer,’s complete workflows with standardized equipment and ,kits, are available to help labs address their SARS-CoV-2 ,testing, challenges. For ,detection,, we offer standardized solutions for isolation of SARS-CoV-2 RNA from various samples types, to automated setup for RNA isolation and PCR, to validated real-time PCR assays.

Medical Device Development Tools (MDDT) | FDA
Medical Device Development Tools (MDDT) | FDA

The FDA’s Medical Device ,Development, Tools (MDDT) program is a way for the FDA to qualify tools that medical device sponsors can use in the ,development, and evaluation of medical devices.

Development & Approval Process | Drugs | FDA
Development & Approval Process | Drugs | FDA

The main consumer watchdog in this system is FDA's Center for Drug Evaluation and ,Research, (CDER). The center's best-known job is to evaluate new drugs before they can be sold.

(PDF) Development Technical Performance and Clinical ...
(PDF) Development Technical Performance and Clinical ...

Development,, Technical Performance, and ,Clinical, Evaluation of a NucliSens Basic ,Kit Application, for ,Detection, of Enterovirus RNA in Cerebrospinal Fluid

Pre-Clinical Development - an overview | ScienceDirect Topics
Pre-Clinical Development - an overview | ScienceDirect Topics

The ,development, of the calanolides is an excellent example of collaboration between a source country (Sarawak, Malaysia), a company (Medichem ,Research,, Inc.) and the NCI in the ,development, of promising drug candidates, and illustrates the effectiveness and strong commitment of the NCI to policies promoting the rights of source countries to fair and equitable collaboration and compensation in ...

PAR-19-253: Focused Technology Research and Development ...
PAR-19-253: Focused Technology Research and Development ...

Early stage technology ,development, can be described in two stages: (I) exploratory proof-of-concept ,research, to determine the best approach(es) for a technology ,development, project, and (II) the subsequent ,research and development, that focuses exclusively on creating and validating a working prototype technology before ,application, to untested biomedical problems is possible.

Medical Device Development Tools (MDDT) | FDA
Medical Device Development Tools (MDDT) | FDA

The FDA’s Medical Device ,Development, Tools (MDDT) program is a way for the FDA to qualify tools that medical device sponsors can use in the ,development, and evaluation of medical devices.

COVID-19 Detection | SARS-CoV-2 Neutralization Antibody ...
COVID-19 Detection | SARS-CoV-2 Neutralization Antibody ...

Global patent protection for the ,kit, will be firmly implemented. 96 well ELISA format test with ACE2 protein attached to the plate and HRP labeled RBD is used for ,detection,. Can be used with serum and plasma samples. The ,kit, comes with positive and negative controls. 4 wells are typically used for the controls, so 92 wells can be used for samples.

SARS-CoV-2 Detection & Research Solutions
SARS-CoV-2 Detection & Research Solutions

PerkinElmer,’s complete workflows with standardized equipment and ,kits, are available to help labs address their SARS-CoV-2 ,testing, challenges. For ,detection,, we offer standardized solutions for isolation of SARS-CoV-2 RNA from various samples types, to automated setup for RNA isolation and PCR, to validated real-time PCR assays.

Applications - Tempus
Applications - Tempus

Research, For clinicians associated with advanced ,research, initiatives, Tempus provides next generation genomic profiling, biological organoid modeling, image/pattern AI recognition, and the full range ,of clinical, trial and ,research, collaborations.

Pre-Clinical Development - an overview | ScienceDirect Topics
Pre-Clinical Development - an overview | ScienceDirect Topics

The ,development, of the calanolides is an excellent example of collaboration between a source country (Sarawak, Malaysia), a company (Medichem ,Research,, Inc.) and the NCI in the ,development, of promising drug candidates, and illustrates the effectiveness and strong commitment of the NCI to policies promoting the rights of source countries to fair and equitable collaboration and compensation in ...

COVID-19 Detection | SARS-CoV-2 Neutralization Antibody ...
COVID-19 Detection | SARS-CoV-2 Neutralization Antibody ...

Global patent protection for the ,kit, will be firmly implemented. 96 well ELISA format test with ACE2 protein attached to the plate and HRP labeled RBD is used for ,detection,. Can be used with serum and plasma samples. The ,kit, comes with positive and negative controls. 4 wells are typically used for the controls, so 92 wells can be used for samples.