APR PCR Certification provides transparency to support a reliable, robust PCR market. Any plastics reclaimer generating PCR pellet or flake can participate in this program to provide customer assurances in the authenticity of their product.Brand companies and converters can commit to using certified PCR to meet sustainability goals and prepare for upcoming regulations

Start Here Find Certified PCR Find an Auditor  Start Here Are you a reclaimer who wants your PCR pellet or flake certified?

 Click on the "Find an Auditor" tab.


Download Pcrs Cert


Download Zip 🔥 https://urluso.com/2y3D1Q 🔥



The below directory is a list of certified PCR available for sale. Any plastics reclaimer generating PCR pellet or flake can participate in the APR PCR Certification program. Seeking guidance on procuring PCR? Check out this helpful guide.

PCRs are necessary tools that define the rules and requirements for creating product category-specific life cycle assessment studies and summarizing the results in Environmental Product Declarations (EPDs) or footprint communications. PCRs are developed openly and collaboratively, much like industry standards. Interested parties and stakeholders may participate in an open development process, which allows them to review the draft PCR, ask questions and share comments electronically. Stakeholders may include material suppliers, manufacturers, trade associations, purchasers, users, consumers, nongovernmental organizations, public agencies, life cycle assessment practitioners and certification bodies.

To move forward with certifying an EPD with UL Solutions, a PCR must already exist for the product type. UL Solutions can certify EPDs using existing PCRs created by any program operator. When no PCR exists for a product group or particular geography, UL Solutions will work with stakeholders to establish one or address regionally specific requirements for existing PCRs created for another market.

Returns the platform configuration register (PCR) value for a specified input file or PEMcertificate. You can use this command to identify the files and signing certificatethat were used to sign an enclave by comparing the command output with PCR values inthe enclave's build measurements.

Specifies the path to the PEM certificate for which to generate PCR8. This option is used to specifically request the PCR8 value by performing deserialisation of the certificate and PEM format validation.

SCS is uniquely qualified to guide you through the exacting, multi-stakeholder PCR development process. Our broad industry expertise stems from over 30 years as a pioneer in environmental claims certification, and as a leading LCA practitioner and developer of advanced LCA methods. Clients include producers of building and construction products, furnishings, food and agriculture, paper, chemicals, electric power generation, and more. SCS is among the first organizations recognized by the ANSI National Accreditation Board (ANAB) as an eligible Program Operator and accredited independent EPD Verifier.

Brand companies and converters looking to fulfill publicly stated sustainability commitments rely on the certainty that the material they are purchasing and incorporating into their packaging is truly PCR. Unfortunately, along with the sharp rise in demand for recycled content, virgin and post-industrial plastics are being fraudulently sold as post-consumer recycled content (PCR). These materials that are marketed or sold as PCR under false pretenses dilute the impact of sustainability commitments, undermine the integrity of the recycling industry, and ultimately weaken trust in recycling as a solution to plastic waste.

What makes it particularly smart or circular? APR PCR Certification provides transparency to support a reliable, robust PCR market and fosters trust at a critical juncture in the plastics packaging value chain. Any plastics reclaimer generating PCR pellet or flake can participate in this program to provide customer assurances in the authenticity of their product. Brand companies and converters can commit to using certified PCR to meet sustainability goals and prepare for upcoming regulations.

Results, Benefits, and Outcomes to Date: At the time of writing, 4 major certifiers have qualified for endorsement by APR to conduct certification audits, and 14 reclaimers offer APR certified post-consumer PET, HDPE, PP, LDPE, LLDPE, LLDR, and MDR resins. Buyers of PCR feel confident that the PCR they are buying is legitimately PCR, and reclaimers with legitimate PCR enjoy an expanded market for their certified PCR.

Food microbiology laboratories can now confidently test to a recognized standard for Salmonella species with the Thermo Scientific SureTect Salmonella Species Assay, which has been granted an NF validation certificate by AFNOR Certification for all foods and pet food.

Global GreenTag certified products pass the world's toughest standards to protect you, and your family's health and safety, minimise your impact on our finite planet and put the power of selection back in your hands.

This certificate is available to matriculated Syracuse University law and graduate students. Interested students are STRONGLY ENCOURAGED to visit the SPL office during the spring semester of their first year to register for the certificate and to discuss a course plan with staff.

If you are looking for Fit to Fly Certificates or COVID-19 Tests for Travel you have come to the right place! In response to the COVID-19 pandemic, many governments and airlines have placed travel restrictions on passengers traveling from the United States. While these travel restrictions are necessary to mitigate the spread of COVID-19, American passengers still need to travel for various reasons. For example, international and non-resident students may desire to return to their home country while university classes are online. Passengers may also need to travel for family emergencies and other life events. For this reason, Medical Care San Diego now offers Fit to Fly certificates for patients who still need to travel during the COVID-19 pandemic. If you need a Fit to Fly certificate, give us a call today! 858-412-6066 **WE ARE ALSO OPEN ON SUNDAYS**

For a Fit to Fly consultation with our physician, please contact your local embassy, travel agency, or airline to determine if there are any specific documents that must be completed by your physician. Please make sure to bring these documents to your consultation to be reviewed and completed by your doctor. Call 858-412-6066 to speak with one of our courteous Patient Representatives to schedule your in-person or virtual consultation with a Medical Care San Diego physician. During this appointment, your doctor will review your recent travel history, medical history, and symptoms. If you meet the criteria for a certification as defined by your country, airline, or travel authority, then your doctor will provide you with a Fit to Fly Certificate that certifies your ability to travel safely. However, if your history does not meet the criteria, you will be referred for COVID-19 testing or follow-up care if needed. Rest assured, our physicians have the health and safety of you and other passengers in mind when issuing a Fit to Fly Certificate. If you have any concerning symptoms of COVID-19 such as cough, fever, sore throat, headache, fatigue, or loss of taste or smell, then we suggest speaking with your primary care doctor or calling 2-1-1 San Diego to schedule a COVID-19 test with a local testing center before visiting our clinic. Please call Medical Care San Diego at 858-412-6066 to schedule your fit to fly consultation today!

Digital polymerase chain reaction (dPCR) is a unique approach to measurement of the absolute copy number of target DNA without using external standards. However, the comparability of different dPCR platforms with respect to measurement of DNA copy number must be addressed before dPCR can be classified fundamentally as an absolute quantification technique. The comparability of four dPCR platforms with respect to accuracy and measurement uncertainty was investigated by using a certified plasmid reference material. Plasmid conformation was found to have a significant effect on droplet-based dPCR (QX100 and RainDrop) not shared with chip-based QuantStudio 12k or BioMark. The relative uncertainty of partition volume was determined to be 0.7%, 0.8%, 2.3% and 2.9% for BioMark, QX100, QuantStudio 12k and RainDrop, respectively. The measurements of the certified pNIM-001 plasmid made using the four dPCR platforms were corrected for partition volume and closely consistent with the certified value within the expended uncertainty. This demonstrated that the four dPCR platforms are of comparable effectiveness in quantifying DNA copy number. These findings provide an independent assessment of this method of determining DNA copy number when using different dPCR platforms and underline important factors that should be taken into consideration in the design of dPCR experiments.

In summary, the relative uncertainty of the partition/droplet volume (type B component) from small to large was as follows: BioMark (0.7%), QX100 (0.8%), QuantStudio 12k (2.3%) and RainDrop (2.9%). The proportion of uncertainty from precision data and the volume of the partition and other sources of uncertainty for all four dPCR platforms were investigated. Results are shown in Figure S3 of the supporting information. The relative amount of uncertainty in the precision data was found to be 93.95%, 87.75%, 43.94% and 20.91% for BioMark, QX100, QuantStudio 12k and RainDrop, respectively. The uncertainty on partition or droplet volume for BioMark, QX100, QuantStudio 12k and RainDrop was 4.92%, 8.74%, 55.44% and 78.16%, respectively. The partition/droplet volume for QuantStudio 12k and RainDrop was successfully measured for the first time. This made it possible to evaluate the uncertainty in the partition volume for these two digital PCR platforms. Uncertainty was greatly decreased by reducing the measurement uncertainty on partition volume for BioMark. As described in an earlier paper1, the z-axis of the partition is the major contributor to the uncertainty of the BioMark partition volume and the uncertainty in the z-axis dimension is attributable both to the limited resolution of the z-axis measurement and the variation in the z-axis dimension across panels. The limited resolution of the z-axis measurement was improved by an alternative measurement: z-axis measurement was treated as a lateral dimension measurement in that the x-z cross sectional was imaged and measured under the microscope by cutting the chip along the x-axis. 2351a5e196

world conqueror 3 apk

cloud foundry client download

carry all my money mp3 download

avc converter download for pc 32 bit

download phone virtual dj