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113705The potency of Extended Insulin Zinc Suspension is based on the sum of its insulin and desamido insulin components, is from 95.0 percent to 105.0 percent of the potency stated on the label, expressed in USP Insulin Units per ml.

113706Aspirin is（）; analgesic; anti-inflammatory.

113707In moist air, Aspirin gradually hydrolyzes to（）and acetic acid.

113708It is（）soluble in ethanol (95) and in acetone, soluble in diethyl ether, and（）soluble in water.

113709Aspirin, when dried, contains（）99.5% of C9H8O4.

113710Aspirin is known as（）.

113711In the British Pharmacopeia, RS stands for:（）.

113712The difference between the titrations represents（）sodium hydroxide required.

113713Boil 0.5 g of the powdered tablets for 2 to 3 minutes with 10 mL of 5 M sodium hydroxide, cool and add an excess of 1　M sulfuric acid; a crystalline precipitate is produced. To a solution of the precipitate in water add iron (III) chloride solution R1; a（

113714Extended Insulin Zinc Suspension shall be stored（）.

113715In the U.S. Pharmacopeia, RS stands for（）.

113716Aspirin Tablets contain Aspirin. It’s content is from 95.0 to 105.0% of the stated amount.

113717The action and use of Aspirin contains the following:Salicylate; non-selective cyclo-oxygenase inhibitor; antipyretic; analgesic; anti-inflammatory.

113718Extended Insulin Zinc Suspension can be repackaged in the unopened multiple-dose container.

113719Extended Insulin Zinc Suspension must be preserved in the opened multiple-dose container provided by the manufacturer.

113720This requirement does not（）countries where exclusive proprietary rights in the name Aspirin are claimed.

113721The tablets（）the requirements stated under Tablets and with the following requirements.

113722It（）in the tests for Sterility and Insulin in the supernatant under Isophane Insulin Suspension and for Zinc content and Zinc in the supernatant under Insulin Zinc Suspension.

113723Extended Insulin Zinc Suspension is modified by the addition of a suitable zinc salt（）such that the solid phase of the suspension is predominantly crystalline.

113724Distribution records shall contain the name and strength of the product and description of the（）, name and address of the consignee.

113725Batch production and control records shall include（）of each batch of component or in-process material used.

113726The persons performing and double-checking the cleaning and maintenance shall date and（）the log indicating that the work was performed.

113727Business places shall have special storage equipment meeting safety provisions for（）medicines.

113728Business places shall have equipment for（）temperature.

113729An important documentation habit for employees of pharmaceutical companies is to ensure that all information recorded by hand is legible.

113730FDA is a governmental agency that is responsible for overseeing the pharmaceutical industry.

113731Results of examinations of documentation in each significant step made in accordance with 211.192.

113732Documentation that each significant step shall have complete labeling control records, including specimens or copies of all labeling used.

113733Warehouses shall provide storage facilities conforming to the national provisions for drugs under special control if they require humidity.

113734Business places shall have special cold storage equipment for drugs requiring refrigeration.

113735For compressed medical gas products, distribution records are not required to contain lot or control numbers.

113736Each time a product is to be made, the operators are issued a copy of the current version of the control record.

113737The drugs under special control shall be provided with the operation facilities meeting the national provisions.

113738Lighting equipment meeting the requirements on storage operation shall be provided for warehouses.

113739Ordinary warehouse shall be established for storage of Chinese herbal medicine.

113740Documentation that each significant step shall include a statement of the actual yield and a statement of the percentage of（）yield at appropriate phases of processing.

113741A batch record is a document that accompanies a（）product as it is made.

113742Business places shall have equipment for storing medicinal slices and（）dispensing for Chinese herbal medicines.

113743If enterprises arrange warehouses, the ground shall be（）.

113744The business places of enterprises shall be appropriate for the operation（）and operation scale of drugs.

113745If the dedicated equipment is employed, the batch record shall also include the records of cleaning,（）, and use.

113746The operators must follow the（）record instructions just as it is written.

113747The following facilities and equipment shall be provided for warehouse, EXCEPT（）.

113748In order to protect the drugs from the impacts of outdoor environment, the business place shall not be（）.

113749Business shall have appropriate（）to protect the drugs from impacts of outdoor environment.

113750Batch production and control records shall include inspection of the packaging and labeling area during use.

113751The control record directs the operators in exactly how to make the product and the operators must follow the batch record instructions just as it is written.

113752Enterprises shall establish the computer system complying with the requirements on operation and quality management.

113753The government formulated some practices to assure the behaviors of enterprises are standardized and orderly.

113754（）shall not be included in the documentation that each significant step in the manufacture, processing, packing, or holding of the batch was accomplished.

113755If enterprises arrange warehouse, the structure of doors and windows shall be（）, and（）safety, protection, and anti-theft measures shall be taken.

113756Entries in the log shall be in（）order.

113757Pharmaceutical industry is a special industry for the people’s（）and（）.

113758Contact someone in pharmaceutical sales　 to find out the possibility of getting a position as a pharmaceutical sales representative.

113759There are restrictions in place to prevent　 materials becoming a bribe.

113760Most powdered medicinal agents require addition of to provide the desired characteristics for tablets manufacture and efficacious use.

113761Dry granulation is especially　 to materials that cannot be prepared by wet granulation.

113762Compressed tablets are manufactured with tablet machines capable of exerting great pressure in　 the powdered or granulated material.

113763Cargo is transported by ship, boat or aircraft but not by containers.

113764Pharmaceutical logistics is a business process without concerning customers.

113765All the doctors always make an appointment with the pharmaceutical sales people first.

113766Tablets are solid dosage forms made by adding some pharmaceutical excipients.

113767Some materials may degrade in moisture or the elevated temperatures required for drying the granules.

113768Weighing and blending the ingredients is the first step of performing wet granulation.

113769The shapes and dimensions of compressed tablets are determined by pressure.

113770Most powdered medicinal agents require addition of excipients such as diluents, binders, disintegrants, and lubricants to determine their shapes.

113771Bringing some promotional materials that come with sales calls can be helpful in making sales.

113772Some doctors prefer to work sales people into their schedules around their patients.

113773The representatives would better establish a good relation with the leaders of the hospitals.

113774is the widely employed method for production of compressed tablets.

113775is not the basic method of manufacturing compressed tablets according to the text.

113776steps are needed to perform the wet granulation according to the text.

113777is thought to be a harm to the relationship between doctors and sales people.

113778All-in-one granulation method mentioned in the text refers to the granulation using .

113779“For this method, either the active ingredient or the diluents must have cohesive properties.”Choose the best translation for the above sentence.

113780is the fourth step of performing wet granulation.

113781The pharmaceutical companies expect their sales reps to .

113782The regulation in pharmaceutical sales refers to .

113783The power mixture is compacted in large pieces and subsequently broken down or sized into granules by .

113784The free-flowing and cohesive properties of some granular chemicals enable them to be directly compressed.

113785The doctors always have plenty of time to communicate with the pharmaceutical sales reps.

113786The widely employed method for production of compressed tablets is direct compression.

113787The sales representative will have to answer the doctors’ questions about the pharmaceuticals.

113788The sales people should bring the presentation　when they intend to visit doctors.

113789also increase material density, improving powder compressibility during tablet formation.

113790In order to , the tablets are conveyed directly from tableting machine to a deduster.

113791are the pharmaceutical customers according to the text.

113792In regional anesthesia, only the area of the body that would feel pain is numbed, allowing the patient to have the procedure while（）.

113793Once the medications are given, a breathing tube is placed into the patient’s airway and connected with a tube to the（）.

113794（）anesthesia is typically used for minor procedures that can be completed in a short time and the patient is expected to return home the same day.

113795The operation rooms are air-conditioned to help prevent（）.

113796Operating rooms are（）environments.

113797Antibiotics are administered to patients after surgery, even if no signs or symptoms of infection are present, in order to prevent this issue.

113798Every patient has complications after surgery.

113799Monitored anesthesia care (MAC), also known as twilight anesthesia, is a type of anesthesia where sedatives are provided to keep the patient calm while allowing the patient to remain awake and responsive.

113800The vast majority of surgeries are performed under general anesthesia.

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