Product Sampling Clause Samples
The Product Sampling clause establishes the terms under which one party provides samples of products to another for evaluation or testing purposes. Typically, it outlines the quantity, quality standards, and delivery method for the samples, as well as any restrictions on their use, such as prohibiting resale or requiring their return after assessment. This clause ensures both parties have a clear understanding of expectations and responsibilities regarding product samples, thereby minimizing disputes and facilitating informed decision-making before entering into larger purchase agreements.
Product Sampling. (a) Schering may provide sampling for the Product for use in the treatment of chronic hepatitis C in a country within the Territory, in reasonable quantities comparable to the sampling conducted for its other anti-viral and/or oncology products in that country; provided, however, that subsequent to commercial launch of the Product in any country, the amount of such sampling in such country shall be limited to [REDACTED]. The free use of Product prior to commercial launch for the treatment of chronic hepatitis C in (i) pre-marketing programs (where permitted by applicable law) and compassionate programs, and (ii) other marketing and Phase IV studies, shall all be deemed sampling of the Product. All samples of the Product shall be purchased at a price equal to [REDACTED].
(b) Subsequent to commercial launch of the Product by ICN in any country, the amount of sampling in such country by ICN shall be limited to [REDACTED]. If the amount of such sampling by ICN in any such country exceeds [REDACTED], then ICN shall pay to Schering an amount equal to the [REDACTED], determined in accordance with the provisions of Section 6.2.
(c) The distribution of Product by Schering during the [REDACTED] preceding the date on which Schering reasonably expects to receive Regulatory Approval shall be consistent with the Research and Development Plan set forth as Exhibit D and with Schering's previous historical compassionate use programs for ribavirin in connection with the treatment of chronic hepatitis C. Schering shall not engage in pre-approval distribution of the Product (other than for clinical trials, which are those with protocols and case report forms) in a manner that could reasonably be expected to compromise the distribution by ICN of the Product in the EU following Regulatory Approval.
Product Sampling. To be eligible to provide product samples to Pavilion visitors, Participant must be participating in the GT Store.
A. Participants may contract for sampling and product demonstration with the GT Store Contractor.
B. Participants offering food samples in the GT Store must comply with Texas Health and Safety Code, Chapter 431, Good Manufacturing Practice regulations, CFR Part 110, and Texas Administrative Code, Chapter 229.183, and provide a manufacturer license number to TDA, if applicable. Applications that do not include a copy of food licenses will not be approved.
C. TDA will provide sampling kiosks or other demonstration areas during approved sampling times.
D. Participants must provide their own sampling or demonstration supplies including napkins, soufflé cups, gloves, toothpicks, etc.
E. All samples provided for consumption must be placed on a napkin, on a toothpick or in a soufflé cup and may not exceed one ounce.
F. Samplings and demonstrations may not in any way interfere with other operations or movement within the Pavilion.
G. All demonstrations must meet health, safety and security standards as set forth in local ordinances and in Fair regulations.
Product Sampling. 3.1 Visual Inspection Each Finished Product lot shall be randomly sampled in accordance with ANSI/ASQ Z1.4, current revision, General, Inspection Level II, Single Normal Sample 0.65 AQL (unless otherwise instructed by Quality Assurance Management), with specific notes for intolerable, major and minor defects (see section 4.0 “Visual Classification of Defects”). Results shall be recorded on appropriate Work Instructions. A lot is defined as the quantity of product processed from one DBM Donor lot and manufactured within a single production record.
3.2 Endotoxin Testing (LAL) LAL test samples, representative of final product, shall be submitted to an approved test laboratory in accordance with section 5.2.
Product Sampling. Do you plan to offer product samples?
Product Sampling. (a) Teva shall ship the Product Samples and either Teva and/or Acorda, as applicable, shall ship Marketing Materials as directed by the Marketing Committee. Each Party shall include an allowance for Product Samples in the forecasts that it provides to the other Party. Acorda and Teva shall be responsible for distributing the Product Samples to their respective sales forces in a timely manner. Each Party shall also be responsible for securing the return and reconciliation of existing Product Sample and Marketing Materials inventories from its discontinued field Sales Representatives. All Product Samples provided to Acorda shall be accompanied by an appropriate Certificate of Analysis and Certification of Release in compliance with the relevant Collaboration Product’s specifications and an indication of expiration dating.
(b) Product Samples supplied by Teva to Acorda shall be used by Acorda solely in connection with the Promotion of the relevant Collaboration Product in the Territory in accordance with the relevant Marketing Plan. Each Party shall be responsible for following its own policies with respect to compliance with the PDMA, and other applicable federal, state and local laws and regulations relating to the distribution and use of Product Samples. Each Party shall be responsible for adherence by its sales force to such laws and regulations, and the Parties shall establish, maintain and adhere to written procedures to assure that each Party and its representatives comply with all requirements of the PDMA. Such written procedures will include a requirement that Acorda notify Teva immediately upon learning that any Product Samples shipped to it have been lost or have not been received as scheduled. Acorda and Teva shall maintain records as required by the PDMA and all other applicable laws. Each Party shall promptly provide the other Party with copies of all its correspondence to and from the FDA and any other regulatory authorities relating to losses and thefts of Product Samples and significant or consistent variances in Product Sample inventory. Each Party will have the right to itself audit the records and/or reports for the Product Samples, as required to be kept by the other Party under the PDMA, during normal business hours, at convenient times and upon no less than five (5) Business Days’ notice.
Product Sampling. To be eligible to provide product samples to Pavilion visitors, Participant must be participating in the Store.
A. All Participants must provide TDA a copy of their current Product Liability Insurance. Participants offering food samples in the Pavilion or Store must comply with Texas Health and Safety Code, Chapter 431, Good Manufacturing Practice Regulations, CFR Part 110, and Texas Administrative Code, Title 25, Part 1, Chapter 229, Subchapter L, Section 229.183, and provide a manufacturer license number to TDA, if applicable. Applications that do not include a copy of current product liability insurance and food manufacturer licenses will not be approved.
B. TDA will provide sampling kiosks or other demonstration areas during approved sampling times. Cancellation or no-show made less than 48 hours in advance of sampling time will incur a $100 per offense cancellation fee to be deducted from final sales and may impact eligibility for future participation.
C. Participants must provide their own supplies including napkins, paper or plastic soufflé cups, gloves, toothpicks, paper towels, cleaning supplies, etc.
D. Participants providing food samples must wear clean, disposable gloves at all times.
E. All samples provided for consumption must be placed on a napkin, on a toothpick or in a soufflé cup and may not exceed one ounce.
F. Samplings and demonstrations may not in any way interfere with other operations or movement within the Pavilion and must be conducted at kiosk during designated times only.
G. All demonstrations must meet health, safety and security standards as set forth in local ordinances and in Fair regulations.
Product Sampling. 3.1 Visual Inspection ****, ****. ****, **** (****,****). Visual inspection shall be performed in accordance with section 4.0.
3.2 (****) ****, ****, ****. ****Certain confidential information contained in this document, marked with four asterisks, has been omitted and filed separately with the Securities and Exchange Commission pursuant to Rule 24b-2 of the Securities Exchange Act of 1934, as amended.
Product Sampling. Safe preparation and handling of food items and samples is very important. If a vendor intends to offer samples of any food products at these events, Safe Food Sampling Guidelines must be followed. Any vendor sampling at the market must bring and use their own handwashing station. Inspectors from MDARD and the Wayne County Health Department are known to stop by from time to time.
Product Sampling. Section 4.5 is hereby amended by deleting from the ---------------- last sentence of that Section the following: * Confidential material omitted and filed separately with the Commission -6- "USB's Cost of Goods and shall be included in the calculation of Operating Profits." and in its place inserting the following: "[ * ] per Vial; provided however, if USB's Cost of Goods materially increases or decreases after the date hereof, the parties shall negotiate in good faith an increased or decreased price for Product for sampling purposes which shall be USB's Cost of Goods plus the amount of the SRI Royalty actually paid by USB to the Southern Research Institute for such Product."
Product Sampling. The awarded Bidder may occasionally be requested by the Department to provide office supply product samples. The purpose of product samples is to ensure quality and conformance to specifications. Describe the Bidder’s ability to conform to these requirements and include any additional quality assurance measures the Bidder will offer.
A. W.
B. ▇▇▇▇▇ will be happy to conduct at no additional cost to the State its own internal audits from time to time as requested by the State on an ad hoc basis as well as taking part in any independent audit that the State may conduct at any time. B. W.