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| Certification Vendor: | Salesforce |
|---|---|
| Exam Name: | Salesforce Certified Agentforce Life Sciences Consultant Exam |
| Exam Number: | ALS-Con-201 |
| Exam Duration: | 105 minutes |
| Real Exam Qty: | 60 scored questions + up to 5 unscored questions |
| Passing Score: | 62% |
| Exam Format: | Multiple-choice, Scenario-based questions, Multiple-select |
| Related Certifications: | Salesforce Certified Data 360 Consultant Salesforce Certified Platform Administrator Salesforce Certified Agentforce Specialist |
| Exam Price: | USD 200 (plus applicable taxes) |
| Available Languages: | English |
| Recommended Training: | Agentforce Life Sciences Consultant Trailhead Path Life Sciences Cloud Customer Engagement Training |
| Exam Registration: | Salesforce Certification Exam Registration Schedule Salesforce Certification Exam |
| Sample Questions: | Salesforce ALS-Con-201 Sample Questions |
| Exam Way: | Online proctored or onsite testing center |
| Pre Condition: | Salesforce recommends experience as a Salesforce Consultant, Architect, Developer, or Business Analyst, plus familiarity with life sciences industry processes. Salesforce Certified Platform Administrator is a required prerequisite. |
| Official Syllabus URL: | https://help.salesforce.com/s/articleView?id=005305357&type=1 |
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NEW QUESTION # 11
Choose 1 option.
Cumulus Pharma requires field sales reps to capture Healthcare Providers' (HCPs) communication preferences during a visit.
What should an Agentforce Life Sciences Consultant configure so reps can view and update consents in the Agentforce Life Sciences mobile app?
Answer: B
Explanation:
Option B is correct because the requirement is specifically about making Consent Management data available in the Life Sciences mobile app. Salesforce Help for Consent Management states that admins must create object metadata cache configuration for supported Consent Management objects and generate a metadata cache so sales reps can view and update consent data. Salesforce also has a dedicated setup topic for creating Object Metadata Cache Configuration, which is accessed from the Life Sciences Commercial app Admin Console under Mobile.
This is important because the Life Sciences mobile app depends on generated metadata cache so that configured objects, fields, and layouts are available to field users on iPad and mobile workflows. Without the metadata cache for the Consent Management objects, reps may not be able to access or update consent preferences during visits, even if the consent model itself is configured correctly.
Option A is not the best answer because Subscription Filtering Fields help control filtering behavior for consent subscriptions, but they do not make the consent objects available in the mobile app. Option C is also incorrect because configuring a desktop Lightning record page does not satisfy the Life Sciences mobile app metadata requirement. Therefore, the consultant should create the object metadata cache configuration for Consent Management objects and generate the metadata cache.
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NEW QUESTION # 12
Choose 1 option.
An Agentforce Life Sciences Consultant at Cumulus Pharma needs to configure Medical Inquiries to ensure a compliant workflow between departments. The requirement states that field sales reps must only be permitted to draft, sign, and submit inquiries, while Medical Science Liaisons (MSLs) must only be permitted to assign and respond to them.
What should the consultant configure on the Medical Inquiry object to enforce these specific user actions?
Answer: A
Explanation:
The correct answer is A from the available options, because the requirement is to control which user actions are exposed to different roles during the Medical Inquiry lifecycle. Salesforce Help for Medical Inquiries states that organizations can define relevant workflow actions for tasks users perform in the medical inquiry process, such as inquiry submission and assignment. Salesforce also describes a compliant role separation where field sales reps can submit medical inquiries, while Medical Science Liaisons can assign and respond to them.
The ideal Salesforce Life Sciences configuration pattern is to use Medical Inquiry workflow actions and workflow paths to control status transitions, actions, and permissions. However, among the provided answer choices, record types with role-specific page layouts is the only option that directly supports restricting the available buttons and actions by user role. This enables sales users to see only draft, sign, and submit actions, while MSL users see only assignment and response actions.
Option B is incorrect because a formula field can calculate or display logic, but it cannot enforce workflow actions or user interaction permissions by itself. Option C is also incorrect because a Flow action could add custom logic, but it is not the standard configuration approach for restricting Medical Inquiry lifecycle actions. Therefore, the best available answer is A.
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NEW QUESTION # 13
Choose 1 option.
Cumulus Pharma requires strict adherence to compliance standards regarding sample inventory. A specialty sales rep needs to perform an unscheduled check of their physical inventory before a site visit. Upon counting, they are physically holding 95 units of "Immunexis 50mg," but the system currently records a balance of 100 units. The sales operations director wants to ensure that, when the rep submits this count, the system follows all compliance guidelines.
Which functionality will meet this requirement?
Answer: C
Explanation:
Option C is correct because an Ad Hoc inventory count assessment is used for an unscheduled inventory check, and Salesforce Life Sciences Sample Inventory Management supports discrepancy adjustments when the counted quantity differs from the system quantity. Salesforce Help states that when a discrepancy is recorded in an inventory count, Sample Inventory Management adjusts the system count positively or negatively to match the actual count. In this scenario, the rep physically counts 95 units while the system shows 100, so the compliant process is to submit the count and let the system create the adjustment transaction for the five-unit negative discrepancy.
Salesforce Help also describes Inventory Count Assessment as the object that captures the overview of the count, including where the assessment occurs and the assessment type. This supports using an inventory count assessment rather than manually changing inventory balances.
Option A is not correct because the missing units were not returned to the distribution center; creating a return would misrepresent the physical inventory event. Option B is also incorrect because an Initial inventory count is used for establishing an initial count, not for reconciling an unscheduled discrepancy after inventory already exists. Therefore, the correct compliant action is to submit an Ad Hoc inventory count assessment and let the system generate the adjustment transaction.
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NEW QUESTION # 14
Choose 1 option.
An Agentforce Life Sciences Consultant is asked to configure strategic distribution limits for Immunexis 50mg in a high-growth territory. The business requirement mandates that the total quantity available for the territory in the next quarter is capped, and individual field sales reps are restricted from handing off more than 50 units in a single visit.
Which administrative configuration should the consultant recommend?
Answer: A
Explanation:
The correct answer is B because the requirement combines two controls: a territory-level cap for a product during a defined period and a per-visit disbursement limit for sales reps. Salesforce Life Sciences documentation for Territory Product Quantity Allocations states that these allocations are used to manage sample product distribution to healthcare professionals, and the setup guidance specifically references the Max Disbursement Limit Quantity as the maximum amount a sales rep can disburse in a given visit.
A Territory Product Quantity Allocation record is designed for the exact scenario described: controlling how much of a specific product is allocated to a territory and limiting how much can be disbursed during a visit. The consultant would define the allocated quantity for Immunexis 50mg for the high-growth territory for the next quarter and set the Max Disbursement Limit Quantity to 50 so that an individual field sales rep cannot hand off more than 50 units in one visit.
Option A is incorrect because setting a product-level maximum sample order quantity would apply too broadly across the organization and would not satisfy the territory-specific allocation requirement. Option C is not the best answer because an Advanced Sample Limit Template at the Healthcare Provider account level controls limits by HCP/account, not the total quantity available to a territory. Therefore, Territory Product Quantity Allocation is the correct administrative configuration.
NEW QUESTION # 15
Choose 1 option.
Cumulus Pharma has configured and activated a new agent using the Life Sciences Field Sales template. However, when a field sales rep attempts to use the agent to generate a summary for a targeted Healthcare Provider (HCP), they are unable to access the feature. Reps must have the privileges required to interact with these capabilities.
Which permission set should the Agentforce Life Sciences Consultant assign to grant access to these Agentforce features?
Answer: B
Explanation:
Option C is correct because Salesforce Help identifies "Access Life Sciences Customer Engagement Agentforce" as the permission required for Life Sciences Customer Engagement Agentforce capabilities. In the Salesforce Help reference for the Life Sciences "Generate Healthcare Provider Summary" action, Salesforce lists the required access as Access Life Sciences Customer Engagement Agentforce. It also notes that, to run flows associated with agent actions, users need the Run Flows app permission or access to the individual flows.
This directly matches the scenario. The Life Sciences Field Sales agent template has already been configured and activated, but the field sales rep cannot use the agent-generated HCP summary capability. That means the issue is not the existence of the agent or the template; it is the user's permission to access the Life Sciences Customer Engagement Agentforce features. Salesforce's Account Summarization permissions documentation also references Access Life Sciences Customer Engagement Agentforce as part of the permission setup for account summarization, alongside standard Life Sciences user permission sets.
Option A, Life Sciences Commercial User, is not specific enough to grant access to these Agentforce capabilities. Option B, Agentforce Service Agent User, relates to Agentforce service use cases and is not the Life Sciences Customer Engagement permission named in the documentation. Therefore, the consultant should assign Access Life Sciences Customer Engagement Agentforce.
NEW QUESTION # 16
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